None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Couples unable to conceive after having regular, unprotected sexual intercourse for >12 months. 2. BMI 3. Husband Semen Analysis within normal references ranges as per WHO 2010 criteria, within last 6 months. 4. Tubal patency documented by HSG/Laparoscopy. 5 Normal Transvaginal ultrasound to exclude any pelvic structural pathology. 6.Genital TB infection ruled out by TB-PCR /BACTEC. 7. Patient consenting to undergo ovulation induction and Intra-uterine insemination treatment
Exclusion criteria
Exclusion criteria: Patients not giving consent or not willing to follow up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the effect of intrauterine instillation of hyaluronic acid enriched media on clinical pregnancy rate in intrauterine insemination treatment.Timepoint: 18 months for recruitment and 6 months for follow up and analysis | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Objectives- 1.To assess the effect of intrauterine instillation of hyaluronic acid enriched media on biochemical and ongoing pregnancy rate up to 20 weeks in intrauterine insemination treatment. 2.To the effect of intrauterine instillation of hyaluronic acid enriched media on miscarriage rate in intrauterine insemination treatment. 3.To estimate patient discomfort and pain following intrauterine instillation using standard pain scale. Timepoint: 18 months for recruitment and 6 months for follow up and analysis | — |
Countries
India
Contacts
AIIMS Jodhpur