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Replantation Following Complete Penile Amputation

NCT06244927 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2024-02-06

No results posted yet for this study

Summary

The goal of this observational study Replantation following Complete Penile Amputation a case series before and after study is to help andrologist and urologists deal with such rare male emergencies easily in emergency situation. There are only limited case reports of penile amputation, a rare urological emergency with a low treatment success rate, and there are still no advanced, detailed surgical or perioperative treatment plans.The main question\[s\] it aims to answer are:

•The investigators used questionnaire to ask participants who undergo replantation surgery to reply. These are the International Index of Erectile Function (IIEF) before and after surgery; the International Prostate Symptom Score (IPSS) estimate for urination after surgery; the Quality of Life index (QoL) estimate, which characterized quality of life into 7 categories: happy (0), satisfied (1), general satisfied (2), not bad (3), not too satisfied (4), distressed (5), and terrible (6). The appearance satisfaction score was based on four levels: from unsatisfactory (1), slight unsatisfactory (2), satisfactory (3) to very satisfactory(4).

Participants (Patients) only need to reply question above. This is observational before and after case study.

Conditions

  • Penile Amputation

Interventions

PROCEDURE

Replantation surgery

Surgery

Sponsors & Collaborators

  • Sir Run Run Shaw Hospital

    lead OTHER

Principal Investigators

  • Hanchao Liu · Sir Run Run Shaw Hospital

Eligibility

Min Age
6 Years
Max Age
58 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-23
Primary Completion
2023-12-20
Completion
2024-01-18

Countries

  • China

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 NCT06244927 on ClinicalTrials.gov