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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05960292
Other study ID # Mohamed Adel Hussien
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2023
Est. completion date April 30, 2024

Study information

Verified date September 2023
Source Egymedicalpedia
Contact Mohamed Adel, MSC
Phone +201065702255
Email elhoseeeeeeny@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Hysterectomy is considered as a common operation in Gynecology. Hysterectomy could be made by vaginally, laparoscopically or abdominally. The American Congress of Obstetricians and Gynecologist advises the use of a minimally invasive technique for the sake of women and to decrease hospital stay and costs.


Description:

Laparoscopic hysterectomy (LH) is a minimally invasive operation that could be made when vaginal hysterectomy is not accessible due to anatomical problems. Vaginal cuff dehiscence (VCD) is a severe adverse event and occurs more frequently after total laparoscopic hysterectomy (TLH) compared with abdominal and vaginal hysterectomy. The study shows effects of the laparoscopic approach versus the vaginal route for the management of vaginal cuff closure during total laparoscopic hysterectomy on female sexual function.


Recruitment information / eligibility

Status Recruiting
Enrollment 56
Est. completion date April 30, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria: 1. Patients who undergo laparoscopic hysterectomy 2. Age ranged from 40 to 80 years. 3. Patients suffering from chronic pelvic inflammatory disease (PID) 4. Dysfunctional uterine bleeding 5. Adenomyosis 6. Endometriosis 7. Fibroid 8. Endometrial hyperplasia 9. Benign ovarian cyst Exclusion Criteria: - Patients with known malignancy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Laparoscopic and Vaginal Hysterectomy
To make a comparison between the Vaginal Vault complications after Hysterectomy

Locations

Country Name City State
Egypt Al-Azhar University hospitals Cairo

Sponsors (1)

Lead Sponsor Collaborator
Egymedicalpedia

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Post operative bleeding (defined as blood loss =500 cc) Amount of lost blood will be measured in terms of assessment of Hemoglobin and Hematocrit levels before and after operation. First 24 hours after The Operations
Primary Postoperative pain Assessment of the pain post-operatively in patients with pain score as : Total scores vary from 0 to 10 in this method, with a higher score indicating more severe pain First 24 hours after The Operations
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