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The aim of this study is to further demonstrate the safety , validity and quality of (sexual)life of vaginal operation for previous cesarean scar defect resection.
Full description
collect all the patients'clinical information,use two questionnaire (the HRQoL and FSFI)to estimate patients' general healthy and sexual function before surgery and postoperation in 1 month,3 months and 6 months
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60 participants in 1 patient group
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Central trial contact
Fan Li, M.D; Chen Shu-Qin, PhD & MD
Data sourced from clinicaltrials.gov
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