Himalaya V-Gel
Benefits of V-Gel: Herbally treats vaginitis and cervicitis
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V-Gel from Himalaya Herbals is a distinctive herbal formula that is effective in the treatment of vaginitis, cervicitis and leukorrhea. V-Gel possesses the antifungal, antibacterial and anti-inflammatory properties and its demulcent action that soothes the inflamed vagina and cervix, relieves itching and accelerates the healing process.
Himalaya V-Gel quells infection and relieves the symptoms such as irritation, burning sensation, dryness and vaginal discharge.
Benefits of V-Gel
V-Gel is helpful when the following symptoms are displayed:
- Vaginitis
- Vaginal candidiasis
- Vaginal trichomoniasis
- Non-specific bacterial vaginitis
- Prevention of post-operative vaginal infections
- Cervicitis
- Leukorrhea
Each gm of V-Gel contains:
Extracts:
- Triphala (Emblica Officinalis, Terminalia chebula, Terminalia bellirica) 4.0mg
- Persian Rose / Satapatri (Rosa damascena Syn. Rosa centifolia) 3.6mg
- Cardamom / Ela (Elettaria cardamomum) 3.6mg
- Spreading Hogweed / Punarnava (Boerhaavia diffusa) 3.6mg
- Stone Flowers / Shaileyam (Parmelia perlata) 2.0mg
- Five Leaved Chaste Tree / Nirgundi (Vitex negundo) 1.6mg
- Turmeric / Haridra (Curcuma longa) 1.6mg
Directions for using V-Gel
Intra-vaginal gel: Apply 1 to 2 gms twice each day with the calibrated applicator (included), for 1 to 2 weeks or till the symptoms are relieved. Wash the applicator with the soap and warm water thoroughly and keep it dry for re-use.
V-Gel Side Effects:
V-Gel is not known to have any side effects if taken as per the prescribe dosage.
V-Gel from Himalaya Herbals
V-Gel is from the renowned Himalaya Herbals brand approved by over 250,000 doctors worldwide and used by customers in over 60 countries. Himalaya Herbals products have been researched clinically and consistent to guarantee bioequivalence. Bioequivalence refers to ensuring that the product on the market is equivalent to the one on which clinical trials were effectively conducted. Himalaya Herbal Healthcare uses chromatographic fingerprinting, one of the most difficult standardization techniques, to ensure consistent quality and performance
V-Gel Research and Clinical Studies:
There have been quite a few studies on the efficacy of V-Gel. The following is one such study.
Evaluation of V-Gel in Vaginitis and Cervicitis
Indu Singh, MD Surya Medi-Tech Hospital and Research Centre, 1, Shivaji Nagar Colony, Mahmoorganj, Varanasi, India.
ABSTRACT
Thirty five females identify with vaginitis, clinically and microbiologically, were enrolled in the study to evaluate the efficacy of V-Gel. Patients were assessed individually for symptoms of vaginal discharge, pruritus, soreness of vulva, inflammation, foul odour and scratch marks. Vaginal discharge was subjected to microbiological diagnosis. The patients were then advised to apply V-Gel with an applicator once daily, at night, for two weeks. At the end of two weeks, a momentous number of patients showed evidence of clinical relief from the 7th day onwards. Thirty patients showed the total inhibition of inflammation of vagina, cervix, vulva and disappearance of scratch marks. Twenty eight patients showed a great reduction in foul odour of the discharge, 25 showed considerable reduction of vaginal discharge, 18 showed relief in soreness and 16 showed relief from pruritus and itching. The results were so optimum at second week where 14 females showed eradication of Trichomonas vaginalis, 15 showed eradication of Candida, 5 showed eradication of Gardnerella vaginalis and one patient showed with eradication of non-specific cocci. Thus, V-Gel considerably produced symptomatic relief and microbiological eradication in patients with vaginitis. Various ingredient of V-Gel have anti-inflammatory and antimicrobial properties that reported to be useful in the treatment of Leucorrhoea. Multiple components of V-Gel have also get produced that synergistic effects with each other as seen from these consequences. Key words: Leucorrhoea, Trichomoniasis, Candidiasis, Vaginitis, Non-specific vaginitis, Cervicitis.
INTRODUCTION
Vaginitis and cervicitis are amongst the most common problems that challenge a gynaecologist. During the menstrual years, the most numerous offenders are Monilia, Candida, Trichomonas vaginalis, Haemophilus vaginalis, etc. In the pre-pubertal and post-menopausal years, the thin vaginal epithelium becomes susceptible to many specific and non-specific organisms. A number of systemic diseases also prompt to vaginitis. Cervicitis is a comparable inflammation of the cervix which can be caused due to improper management during labor or may be a so much consequence of mounting infection during vaginitis. A patient with vaginitis or cervicitis is posed with a number of symptoms those such as leucorrhoea (excessive vaginal discharge), vulvar itching and irritation, which are not only awkward but also cause immense discomfort and hindrance to normal daily activities.
Due to the frequency of this infection and the general problem of recurrence, several treatment schemes have been used over the years. While the exploit of substance such as vaginal douches, Betadine, etc. is beneficial, their action, conversely, is short-lived. Systemic administration of metronidazole and other drugs al though effective, have side effects and are not arranged for pregnant women. These limitations necessitate a safer and more efficient remedy in this field.
Ayurveda, the esteemed Indian system of medicine, with its copious herbal remedies, has provided a number of combination preparations for various confusion with little or no side effects. V-Gel, comprising extremely potent herbs like Berberis aristata, Boerhaavia diffusa, Vitex negundo, Lawsonia inermis, Azadirachta indica and Cedrus deodara, is a formulation which is analogous to modern medicine and used for vaginal infections. It has exhibited considerate antimicrobial and antifungal action in experimental trials. Its effect on skin and mucosal inflammation has been proved by different studies conducted on animals and no side effects have been reported that . It is safely used during pregnancy.
MATERIAL AND METHODS
Thirty five female patients between the age of 20-55 years were incorporated in the trial. All the patients had clinical signs and symptoms of vaginitis and cervicitis. These were patients with the leucorrhoea, inflammation of vulva, foul odor, pruritus and soreness. Complete medical, gynaecological and obstetrical examinations of all patients were carried out to rule out any support of malignancy and genetic disorders to exclude them from the trial. A positive microbiological diagnosis was also inveterate in all the patients.
Patients were advised to apply V-Gel once every day at night (before retiring to bed) with an applicator for two weeks.
The patients were all examined on the 7th, 14th and 21st days to assess symptomatic relief. A microbiological test was frequent on day 14 for microbiological evidence of cure and followed up for 21 days to determine the degree of remedial response as complete relief, partial relief or no response.
All the patients were all advised to observe abstinence during the study period. This was an release clinical trial using V-Gel on all the patients for assessing clinical response on post-treatment.
Relief into clinical symptoms (pruritus, soreness, discharge and inflammatory signs along with reduction in microbiological count) was considered best as the criteria of efficacy. Follow-up was done two times weekly for three weeks to note if any side effects occurred with topical application of vaginal gel. Patients were also chase up for the next 3 months to note the recurrence of symptoms and prerequisite of other therapeutic drugs, if necessary.
RESULTS
Thirty five patients with clinical signs and indication of vaginitis were included and all of them completed the trial. At the end of two weeks, the results were analyzed. Thirty patients showed relief from the inflammed vagina, vulva, cervix and scratch marks on the 7th day. Twenty eight patients showed upgrading in foul odour and 25 showed important reduction of vaginal discharge. Eighteen patients showed improvement in soreness and 16 got relief from pruritus and itching. On day 15, all the patients showed support of anti-inflammatory effects on the vulva, vagina and cervix, 33 showed relief from scratch marks, 31 showed a diminution of vaginal discharge, 30 showed disappearance of foul odour, 28 experienced relief from the itching and pruritus and 23 displayed disappearance of soreness.
DISCUSSION
Vaginal gel on topical application was found very efficient in relieving signs and indication of vaginitis caused by multiple organisms. Application of the gel for two weeks had no adverse side effects. There was a significant lessening of vaginal discharge in 75.75% patients on day 7 and 93.93% on day 15. Similarly foul odour summary in 93.33% on day 7 and 100% on day 15.
The quantity and odour of the vaginal discharge are two significant clinical symptoms of vaginitis, which were relieved by the vaginal gel after the two weeks of topical application.
Pruritus and itching are also vital clinical symptoms of vaginitis in all age groups of patients, which were relieved in the 51-61% on day 7 and 90.32% on day 15. The relief from pruritus is major and is confirmed by the disappearance of scratch marks in 90.90% on day 7 and 99% on day 15. Vaginal and cervical soreness disappeared in 72% on day 7 and 92% on day 15. Vaginal and cervical inflammation was also considerably reduced in 85-71% on day 7 and 100% on day 15. Thus, the vaginal gel has shown powerful anti-inflammatory and anti-infective activity in patients with virginities.
Its antimicrobial properties are incorrigible by its effect on vaginal and cervical flora on microscopic examination of cervical flora. 66.66% showed fading of Trichomonas vaginalis on day 7 and 88.88% on day 15. Candida albicans also disappeared in 88.20% on day 15. The effect of V-Gel on Candida albicans was found regular as only 45.57% were eradicated by day 7. Gardnerella vaginalis was eradicated 100% by day 7. Non-specific organisms were stamp out on day 7 in 50% and 100% on day 15.
Partial cure of signs and symptoms were seen in 94.28% on day 7 and 80% were completely cured on day 21 (Table 3).
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