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NCT04376086 Clinical Trial

Segmental Epidural Block for Feeding Jeujunostomy in Cancer Patients

Anesthesia Clinical Trial

Official title:
Segmental Epidural Block for Feeding Jejunostomy in Cancer Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04376086
Other study ID # AP1904-50103
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 10, 2019
Est. completion date April 26, 2021

Study information
Verified date May 2021
Source National Cancer Institute, Egypt
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aim is to compare the efficiency and safety of segmental epidural block versus general anesthesia in cancer patients undergoing surgical feeding jejunostomy

Description:

Comparing general anesthesia versus segmental epidural anesthesia in feeding jejunostomy

Recruitment information / eligibility
Status Completed
Enrollment 44
Est. completion date April 26, 2021
Est. primary completion date April 25, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients scheduled for surgical feeding jejunostomy more than 18 years old Exclusion Criteria: - patien refusal Coagulation defect Abnormal kidney or liver functions Local infection at site of block Bone metastases

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Epidural anesthesia
Segmental epidural analgesia
• general anesthesia
general anesthesia

Locations
Country Name City State
Egypt National Cancer Institute Cairo

Sponsors (1)
Lead Sponsor Collaborator
National Cancer Institute, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Analgesic requirements Analgesic requirments first 24 hours
Primary Haemodynamics blood pressure periooperative time
Secondary VAS score visual analouge scale 0 minimum to 10 maximum score 24 hours
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