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NCT05373238 Clinical Trial

Same Day Discharge After Laparoscopic Hysterectomy

Surgery--Complications Clinical Trial

Official title:
Same Day Discharge After Laparoscopic Hysterectomy vs Late Discharge

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05373238
Other study ID # BVU-10.2021
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 15, 2021
Est. completion date April 30, 2022

Study information
Verified date October 2022
Source Bezmialem Vakif University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients who are scheduled for laparoscopic hysterectomy will be included in the study. After the operation, those who are well and without major distress will be discharged from the hospital before 24 hours. Those who have pain or have additional health problems will be observed further. Our aim is to compare these two groups in terms of early complications and operation characteristics.

Recruitment information / eligibility
Status Completed
Enrollment 194
Est. completion date April 30, 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers
Gender Female
Age group 35 Years to 80 Years
Eligibility Inclusion Criteria: - Patients Scheduled For Hysterectomy Exclusion Criteria: - Diagnosis of Malignancy - Those with intraoperative complication

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Early discharge
Early discharge

Locations
Country Name City State
Turkey Bezmialem Vakif University Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Complication in 30 days Number of patients with surgical complications, postoperative complications, wound complications 30 days
Secondary Postop hb Number of patients whose hemoglobin value declined beyond two parameters. (mg/dL) 30 day
Secondary Postop htc Number of patients whose hematocrit value declined more than 5 percent (%) 30 day
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