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Role of medical therapyfor preventing malignant changes in high risk molar pregnancy

Phase 3
Conditions
Health Condition 1: null- Patients with high risk molar pregnancy
Registration Number
CTRI/2017/09/009723
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

60 patients with pelvic ultrasound showing complete mole having serum beta human chorionic gonadotrophin more than 100000 IU/L,uterine size larger for dates,presence of bilateral theca lutein cysts

Exclusion Criteria

partial mole,histological evidence of chorio ca,previous history of molar pregnancy,total leucocyte count less than 2500/mm3,neutrophil count less than 1500/mm3,SGOT more than 50IU/ml

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
effect of methotrexate on duration of normalisation and regression pattern of serum beta hcgTimepoint: with in 8 weeks of evacuation
Secondary Outcome Measures
NameTimeMethod
Incidence of GTD in patients receiving chemoprophylaxisTimepoint: serum beta hcg more than 20,000mIU/ml after 4 weeks of evacuation,raised beta hcg after 6 months of evacuation
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