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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04033471
Other study ID # 464
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date July 1, 2019
Est. completion date April 2021

Study information

Verified date February 2021
Source Assiut University
Contact Shereen M Kamal, Associate proferssor
Phone 01006279209
Email sheridouh79@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study aim to Compare the effect of preoperative Epidural Midazolam, Morphine and their combination in postoperative pain relief and total morphine consumption.


Description:

Major abdominal surgeries with abdominal incisions lead to severe abdominal pain, which if treated inadequately, can cause shallow breathing, atelectasis, retention of secretions and lack of cooperation in physiotherapy. This increases the incidence of post-operative morbidity and leads to delayed recovery.Epidural anesthesia is safe and inexpensive technique with the advantage of providing surgical anesthesia and prolonged postoperative pain relief. It also an effective treatment of operative pain blunts autonomic, somatic and endocrine responses. Morphine and midazolam can be used as adjuvant to bupivicain to reduced the postoperative pain


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date April 2021
Est. primary completion date March 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - ASA I-II patients scheduled for major abdominal cancer surgeries Exclusion Criteria: - patients with known allergy to the study drugs, - significant cardiac, respiratory, renal or hepatic disease, - drug or alcohol abuse, - psychiatric illness that would interfere with perception and assessment of pain.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
midazolam
epidural needle in the L1-2 or L2-3 space , and using loss of resistance technique udder strict aseptic condition 10 ml of the prepared drug will be given

Locations

Country Name City State
Egypt Assiut University Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary time to first request of analgesia the time between the end of operation and tracheal extubation to the first request for supplemental analgesics and its administration to the patient 1st 48 hours postoperative
Secondary the cumulative consumption of morphine in the 1st 48h postoperatively total amount of morphine used for analgesia 1st 48 hours postoperative
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