Study of Different Therapeutic Strategies in Hydatidiform Mole With Lung Nodule

NCT03785574 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-03-16

No results posted yet for this study

Summary

The purpose of present study is to provide clinical evidences for the appropriate management of molar pregnancy with lung nodule. The hydatidiform mole patients with lung nodule ≥1.0cm will be randomized into 2 groups: A. treated with chemotherapy immediately, B. follow up until hCG level met FIGO diagnostic criteria of GTN (B1) or hCG level declined to normal spontaneously (B2). Lung nodule \<1.0cm will directly treated as group C

Conditions

  • Hydatidiform Mole
  • Gestational Trophoblastic Neoplasia

Interventions

OTHER

Follow up

the follow up group would be naturely didived into 2 subgroups depending the hCG regression degree.

DRUG

chemotherapy

First line treatments:low risk:Methotrexate or ACTD; high risk:EMA-CO

Sponsors & Collaborators

  • Qilu Hospital of Shandong University

    collaborator OTHER
  • Tongji Hospital Affiliated to Tongji Medical College of HUST

    collaborator UNKNOWN
  • The First People's Hospital of Yunnan

    collaborator OTHER
  • Tianjin Central Hospital of Gynecology Obstetrics

    collaborator OTHER
  • Women and Children's Hospital of Ningbo University

    collaborator UNKNOWN
  • First Affiliated Hospital of Wenzhou Medical University

    collaborator OTHER
  • Hangzhou Fuyang Women And Children Hospital

    collaborator UNKNOWN
  • Zhejiang Provincial Tongde Hospital

    collaborator OTHER
  • Shaoxing Shangyu Women And Children Hospital

    collaborator UNKNOWN
  • Huzhou Maternity and Child Health Care Hospital

    collaborator UNKNOWN
  • Women's Hospital School Of Medicine Zhejiang University

    lead OTHER

Principal Investigators

  • Xing Xie · Women's Hospital, Zhejiang University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-24
Primary Completion
2030-09-01
Completion
2030-09-01

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03785574 on ClinicalTrials.gov