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A clinical trial to study the effects of two different protocols of cetrorelix injection timings in IUI cycles in infertile women

To compare the efficacy of two different regimens of GnRH antagonists in clomiphene-Gonadotropin induced controlled ovulation and IUI cycles

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/12/005289
Enrollment
45
Registered
2014-12-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Infertility

Interventions

Intervention1: clomiphene-gonadotropin ovulation induction cycles with Cetrorelix: Cetrorelix as 0.25mg subcutaneously is the intervention drug studied in two different regimens given in clomiphene ci

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Unexplained infertility; 2)Mild male factor infertility; 3)Ovulation dysfunction infertility with previously failed induction with letrozole or clomiphene; 4)At least one patent fallopian tube; 5)BMI 18.5â??29.9 kg/m2 6)Euthyroid state 7)No associated medical problems like diabetes mellitus or Hypertension or Drug allergies.

Exclusion criteria

Exclusion criteria: 1)Severe male factor infertility; 2)Stage III or IV endometriosis; 3)Tubal Factor Infertility; 4)baseline FSH >12 IU/L; 5)Less than four antral follicles per ovary

Design outcomes

Primary

MeasureTime frame
1.Premature luteinization rate 2.Ovulation ratesTimepoint: 1. If LH more than 10 mIU/ml and Progesterone more than 2ng/ml on day 10 and/or day 12 of menstrual cycle 2. Documented by transvaginal ultrasound after 36 hours of ovulation trigger

Secondary

MeasureTime frame
1.Pregnancy rate 2.Endometrial thickness 3.Adverse effects like ovarian hyperstimulation syndrome and multiple pregnancies 4.Cycle cancellation rate Timepoint: 1.Positive urine pregnancy test after 15 days of IUI 2.Thickness measurement on the day of dominant follicle (more than or equal to 18 mm size) 3.Checked on the day of positive urine pregnancy test or in a symptomatic patient 4.If no dominant follicle by day 18 of the cycle

Countries

India

Contacts

Public ContactDr Devendra siva karthikS

All India Institute of Medical Sciences

garimakachhawa2012@gmail.com09868246702

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026