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Comparing Two Types of Estrogen Therapy in Diagnosed Cases of Premature Ovarian Insufficiency.

Comparing The Effect Of Estradiol Valerate And Conjugated Equine Estrogen In The Patients With Premature Ovarian Insufficiency A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068270
Enrollment
60
Registered
2024-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: N911- Secondary amenorrhea

Interventions

Intervention1: Oral estradiol valerate along with oral medroxy progesterone acetate.: Oral estradiol valerate 2mg daily along with oral medroxy progesterone acetate 10mg from day 15- day 25. Control

Sponsors

Guru Teg Bahadur Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All the women below 40 yrs with newly diagnosed POI according to ESHRE guidelines

Exclusion criteria

Exclusion criteria: 1.Patient with chromosomal anomalies 2.Already receiving or have received hormone therapy. 3.Hormone therapy is contraindicated like in : a) Known case or history of breast cancer and uterine cancer. b) Active or history of deep venous thrombosis (DVT) or pulmonary embolism. c) History of clotting disorder d) Active or history of arterial thrombotic diseases such as myocardial infarction or stroke e) Chronic liver disease or dysfunction f) Migraine with aura 4. Have received non-hormonal treatment like SSRIs, Gabapentinoids or Neurokinin B for

Design outcomes

Primary

MeasureTime frame
1)Comparison between the changes in clinical parameters among two groups after 6 months of HRT. 2)Comparison between changes in radiological parameters among two groups after 6 months of HRT. 3)Comparison between changes in biochemical parameters among two groups after 6 months of HRT.Timepoint: 6months

Secondary

MeasureTime frame
Comparison of side effects of HRT among two group which will include liver function tests.Timepoint: 6 months.

Countries

India

Contacts

Public ContactRitam Kumari

University College Of Medical Sciences And GTB Hospital

rachna_anila@yahoo.co.in9123409954

Outcome results

None listed

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