Assessing the Psychosocial Burden in Women With an Abnormal Pap Results After Screening Interventions

NCT00520117 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 151

Last updated 2019-09-30

No results posted yet for this study

Summary

The primary purpose of this study is to assess the psychosocial burden in women who have experienced an abnormal pap results after screening interventions.

Conditions

  • Papanicolaou Smear

Sponsors & Collaborators

  • Mahidol University

    lead OTHER

Principal Investigators

  • Punnee Pitisuttithum, Professor · Department of Clinical ITropical Medicine, Faculty of Tropical Medicine, Mahidol University

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2008-06-30
Completion
2008-06-30

Countries

  • Thailand

Study Locations

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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 NCT00520117 on ClinicalTrials.gov