A comparative study of lashuna taila and narayana taila uttarbasti in the treatment of female infertility

Phase 2

Not yet recruiting

• Conditions: Chronic salpingitis and oophoritis. Ayurveda Condition: VANDHYA,

• Registration Number: CTRI/2025/06/089222
• Lead Sponsor: State ayurvedic College and Hospital Lucknow

Brief Summary

this is a randomised comparative clinical study phase 2 parallel group trial . Comparing the efficacy of Lashuna taila uttarbasti and Narayana taila uttarbasti in case of stri bandhyattava for 3 months in 30 patients . The patient fulfilling the cclinical criteria for diagnosis of stri bandhyattava will be randomly selected from OPD / IPD of State Ayurvedic College and Hospital Lucknow and referred cases from other hospitals . a careful history , physical examination and necessary investigations will be performed . further patients divided into two groups , Group A- patient will be treated with Lashuna taila uttarbasti in the dose 3-5 ml through transvaginal route after cessation of menses for 3 alternative days for 3 consecutive cycles in Group B - patient will be treated with Narayana taila uttarbasti in the dose of 3- 5 ml through transvaginal route after cessation of menses for 3 alternative days for 3 concsecative cycles . Follow up period after 30 days with trial drug and last follow up after 30 days of completion of trial.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2025-06-14
• Study Start: 2025-06-25

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

• 1.Married women with Age between 21 to 40 years.
• 2.Patient of primary and secondary infertility 3.Clinically diagnosed Patients of unilateral or bilateral tubal blockage.

Exclusion Criteria

• 1.Patient with active and chronic pelvic infections.
• 2.Patient of any Genital organ diseases like- Uterine fibroid.
• Genital Prolapse Endometriosis, Adenomyosis etc.
• 3.Patient with history of hypdrosalpinx.
• 4.Women of age less than 21 and above than 40.
• 5.Other systemic disorders like hypertension, diabetes, tuberculosis.
• 7.Patient having organic pathology of uterus and adnexal like cervical carcinoma, Cervical Intraepithelial Neoplasia (CIN).
• And any malignant growth.
• 8.HIV, VDRL, HBsAg positive patient.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
to evaluate the efficacy of lashuna taila and narayana taila uttarbasti in management of tubal blockage	after 30 days | after 30 days | after 30 days | after 30 days of trial
Improvement in tubal patency	after 30 days | after 30 days | after 30 days | after 30 days of trial

Secondary Outcome Measures

Name	Time	Method
Conception / pregnancy rate	Reduction in associated symptoms of bandhayyatava

Trial Locations

Locations (1)

State Ayurvedic College and Hospital Tulsidas marg Turiyaganj Lucknow; 🇮🇳 Lucknow, UTTAR PRADESH, India

State Ayurvedic College and Hospital Tulsidas marg Turiyaganj Lucknow

🇮🇳Lucknow, UTTAR PRADESH, India

Dr Gulafshan

Principal investigator

7905628653

khangulafshan80@gmail.com