Clinical TrialID 8399

Efficacy of Ultrasound Guided PIFB Versus Lidocaine Infusion on Postoperative Pain After Thoracotomy

NCT05885230

Cardiac Surgery

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
8399
Evidence Id
8399
Core Evidence Id
8399
Source Clinical Trial Id
8397
Herb2 Clinical Trial Id
HBCT008397
Nct Id
NCT05885230
Title
Efficacy of Ultrasound Guided PIFB Versus Lidocaine Infusion on Postoperative Pain After Thoracotomy
Status
Recruiting
Phase
Study Result
No
Study Condition
Cardiac Surgery
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: SINGLE (PARTICIPANT)|Primary Purpose: PREVENTION
Intervention
PROCEDURE: pecto intercostal fascial block using bupivacaine 0.25%|DRUG: lidocaine infusion
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Single
Intervention Purpose
Prevention
Gender
All
Age
Adult, Older_Adult
Enrollment
138
Outcome Measure
Total dose of morphine in the first 24 h postoperatively., total morphine consumed in the first 24 hour, 24 hours postoperative
Sponsor Collaborator
Beni-Suef University
Funded By
OTHER
Location
Benisuef University Hospital, Banī Suwayf, e\EYGPT, Egypt
Other Id
FMBSUREC/09042023/Mikhael
Start Date
2023-05-01
Primary Completion Date
2024-05
Completion Date
2024-05
First Posted
2023-06-01
Results First Posted
Last Update Posted
2024-04-10
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05885230
Title Cn
Title En
Efficacy of Ultrasound Guided PIFB Versus Lidocaine Infusion on Postoperative Pain After Thoracotomy
Bilingual Status
semi_complete