Intertransverse Process Block to Improve Quality of Recovery and Pain Management in Adult Cardiac Surgical Patients
Recruiting
N/A
Interventional Study
Chronic Postsurgical Pain
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 96 (estimated)
- Sponsor
- Chinese University of Hong Kong · Other
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About This Trial
The goal of this clinical trial is to evaluate the efficacy of intertransverse process block (ITPB) in improving quality of recovery and potentially preventing chronic postsurgical pain (CPSP) in adult patients undergoing elective cardiac surgery (e.g., coronary artery bypass graft \[CABG\], valve repair/replacement, or combined CABG/valve procedures).
The main questions it aims to answer are:
1…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* adult patients aged 18 or older
* undergoing elective CABG, valve repair/replacement, or combined CABG/valve procedure via sternotomy
Exclusion Criteria:
* Emergency surgery
* redo surgery
* history of chronic pain or being on chronic opioids/sedatives
* renal failure with a…
Contacts