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Post-mastectomy Pain Syndrome clinical trials

View clinical trials related to Post-mastectomy Pain Syndrome.

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NCT ID: NCT06443619 Not yet recruiting - Clinical trials for Post-mastectomy Pain Syndrome

Efficacy of Glucose in Serratus Anterior Plane Block to Reduce the Occurrence of Chronic Post-mastectomy Pain

Start date: June 4, 2024
Phase: N/A
Study type: Interventional

Nearly 50% of patients suffer from chronic pain following breast cancer surgery. Several regional anesthesia techniques, including paravertebral block, erector spinae plane block, pectoral nerves block, and serratus anterior plane block, have been applied for acute pain control and prevention of chronic pain after breast cancer surgery. Exploiting the beneficial effect of glucose in regulating neuroinflammation and neuropathic pain, we hypothesize that the addition of glucose to bupivacaine could be superior to bupivacaine in ultrasound-guided SAPB in improving the quality of postoperative analgesia and preventing chronic pain after mastectomy. Patients will be randomly allocated into one of two equal groups (30 patients each ); the study group; Group I( B-D) (n=30): will receive unilateral USG-deep SAPB 0.4 ml/kg Of 0.25 % isobaric bupivacaine with addition of 15ml glucose 5% to (30 ml total volume); Group (B-N) (n=30): will receive unilateral USG-deep SAPB 0.4 ml/kg Of 0.25% isobaric bupivacaine to be diluted with 15ml isotonic saline (30 ml total volume). The occurence of postmastectomy pain, 3 months after surgery, will be the primary outcome.

NCT ID: NCT04989179 Not yet recruiting - Breast Cancer Clinical Trials

Incidence and Factors Affecting the Development and Outcome of Post Mastectomy Pain Syndrome

PMPS
Start date: August 2021
Phase:
Study type: Observational

Phase 1 of this multi-centre, prospective study aims to obtain a precise estimate of the local incidence of PMPS and identify biopsychosocial risk factors contributing to the development of PMPS. Recognition of the impact of PMPS on function and mood and quality of life in cancer survivors, and identification of risk factors would help physicians institute appropriate pre-operative counselling and preventive measures to reduce the development of PMPS. The investigators aim to follow up on the long-term multi-dimensional effects of PMPS, and continue to develop and validate a risk prediction model for patients at risk of PMPS in the next phase of the study.

NCT ID: NCT04317898 Not yet recruiting - Clinical trials for Post-mastectomy Pain Syndrome

Ultrasound-Guided Serratus Plane Block Vs Paravertebral Block For Chronic Post-mastectomy Pain.

Start date: July 2020
Phase: N/A
Study type: Interventional

compare the analgesic efficacy between ultrasound paraverbral block and serratus block in post mastectomy pain.