RISS Versus SPSIP Block in Modified Radical Mastectomy
Recruiting
N/A
Interventional Study
Postoperative Pain
Breast Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 75
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 80 (estimated)
- Sponsor
- Ferit Yetik · Government
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About This Trial
This prospective randomized double-blind controlled trial aims to compare the postoperative analgesic efficacy and dermatomal spread of rhomboid intercostal-subserratus plane (RISS) block and serratus posterior superior intercostal plane (SPSIP) block in patients undergoing modified radical mastectomy. Postoperative pain scores, opioid consumption, rescue analgesic requirements, block-related comp…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female patients aged 18-75 years
* ASA physical status I-III
* Scheduled for elective unilateral modified radical mastectomy with axillary dissection under general anesthesia
* Provision of written informed consent
Exclusion Criteria:
* Anticoagulant therapy
* Bleeding diath…
Contacts