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Efficacy of Letrozole as priming agent in First trimester MTP.

Efficacy of Letrozole pretreatment prior to Misoprostol in first trimester Medical Termination of Pregnancy- A prospective clinical study. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105751
Enrollment
120
Registered
2026-03-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: O021- Missed abortion Health Condition 2: O029- Abnormal product of conception, unspecified

Interventions

Intervention1: T.LETROZOLE + T.MISOPROSTOL: T.LETROZOLE 10mg orally once daily from Day 1 to Day 3 followed by on Day-4- Misoprostol 800 mcg sublingually, single dose. (T.Letrozole 10mg will be given

Sponsors

SOUNDHARYA V
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women age 18 yrs and above. Confirmed intrauterine pregnancy upto 9 wks /63 days (based on Ultasound findings). Indications for Termination as per MTP Act . Hemoglobin levels greater than 10g/dl. Willing to participate and provide written and informed consent.

Exclusion criteria

Exclusion criteria: Hypersensitivity to Misoprostol/ Letrozole. Multiple pregnancy. Uterine anomalies. Bronchial asthma. Steroid hormone dependant cancer. Systemic diseases. Coagulopathies/Thromboembolism. Suspected ectopic or Molar pregnancy. Porphyria. Severe or recurrent Liver disease or Pruritis of Pregnancy. Breast feeding. Acute illness of any nature.

Design outcomes

Primary

MeasureTime frame
To compare induction abortion interval and rate of complete abortion without the need of surgical intervention between study (LETROZOLE+MISOPROSTOL) and control groups (MIFEPRISTONE+MISOPROSTOL) . Timepoint: Baseline,Day-3,Day-4,Day-5,Day-6

Secondary

MeasureTime frame
To assess total duration of vaginal bleeding during abortion in both the groups & to make comparison between study & control groups. To assess side effects & complications in both the groups. To evaluate patient satisfaction & tolerability of the regimen in both the groups .(Graded as Satisfactory/Unsatisfactory) Timepoint: Baseline,Day-3,Day-4,Day-5,Day-6

Countries

India

Contacts

Public ContactSOUNDHARYA V

GOVERNMENT RAJAJI HOSPITAL , MADURAI

nubraganga@gmail.com9443924974

Outcome results

None listed

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