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Oral natural micronized progesterone sustained release formulation as a support for luteal phase

A Prospective observational study of oral natural micronized progesterone sustained release formulation as luteal phase support - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/078124
Enrollment
50
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: N998- Other intraoperative and postprocedural complications and disorders of genitourinary system

Interventions

Intervention1: NIL: NIL

Sponsors

Alembic Pharmaceuticals Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Woman ready to give informed consent for participation in study.

Exclusion criteria

Exclusion criteria: a. Women with history of Progesterone (Natural or synthetic) use in the last 3 months b. History of tubal insufficiency or obstruction including Endometriosis or Polycystic Ovarian Syndrome, c. History of AST and, or ALT greater than 2.5 x ULN (active liver disease), d. History of Serum creatinine greater than 1.5 mg per dl (active renal disease), e. History of Uncontrolled hypertension, hypercholesterolemia or diabetes, f. History of Psychoactive disease or on antidepressants, g. History of Smoking h. History of Myocardial infarction, stroke, cardiovascular or circulatory or clotting disorders i. History of Oral anticoagulants or prolonged use of high doses of NSAIDs, j. Hypersensitivity to Natural micronized progesterone k. Any condition that, in the opinion of the investigator, does not justify the patient’s inclusion in the study

Design outcomes

Primary

MeasureTime frame
Serum Progesterone(P)levels(ng/ml)Timepoint: Day 0 and Day 5

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactPallavi Singh

Rajendra Nagar Hospital and IVF center

apgl2015@gmail.com9415405091

Outcome results

None listed

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