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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: NCT06087211 Recruiting - Clinical trials for Post-mastectomy Pain Syndrome

Pain Relieving Potentials of Combination of Oral Duloxetine and Intravenous Magnesium Sulphate in Post Mastectomy Pain

Start date: October 10, 2023
Phase: Phase 4
Study type: Interventional

This study aims to evaluate the effect of combined duloxetine and IV Magnesium sulphate to decrease acute and chronic post mastectomy pain. The study will be conducted in National Cancer Institute and all the participants will be enrolled from female patients scheduled for modified radical mastectomy under general anesthesia in National Cancer Institute, Cairo University.

NCT ID: NCT05935059 Recruiting - Clinical trials for Post-mastectomy Pain Syndrome

The Efficacy of Tianeptine Versus Pregabalin on Acute and Chronic Post Mastectomy Pain After Breast Cancer Surgery.

Start date: June 21, 2023
Phase: N/A
Study type: Interventional

Breast cancer is the most common malignancy among females. Nearly 40% of breast surgery patients experience moderate to severe acute postoperative pain, with severe pain persisting for more than 6 months in almost 20-50% of patients (post mastectomy pain syndrome) which is defined according to International Association for the Study of Pain (IASP) as pain which persists more than 3 months after mastectomy/lumpectomy affecting the anterior thorax, axilla, and/or medial upper arm. Different pharmacological tools have been in use for either prevention or treatment of such refractory pain syndrome with variable efficacy. The aim of this study is to assess the efficacy of the perioperative use of Pregabalin versus Tianeptine on the emergence of PMPS in female patients undergoing MRM for breast cancer.

NCT ID: NCT05771103 Recruiting - Clinical trials for Post-mastectomy Pain Syndrome

Stellate Ganglion Destruction With Alcohol Versus Thermal Ablation for Chronic Post Mastectomy Pain

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

- Group A: SGB with alcohol injection by ultrasound guidance and C7 level confirmation by fluoroscopy. - Group B: Thermal RF; thermal RF neurolysis will be applied with a time of 60 seconds at 80º C, and then will be repeated twice . Stellate ganglion RF therapy will be done under fluoroscopy, integrated by ultrasound guidance

NCT ID: NCT05770596 Recruiting - Clinical trials for Post-mastectomy Pain Syndrome

Vitamin C on Acute and Chronic Post Mastectomy Pain

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

This prospective randomized double-blinded controlled study will be conducted to evaluate the effect of perioperative vitamin C on acute and chronic post mastectomy pain after breast cancer surgery

NCT ID: NCT05458154 Completed - Clinical trials for Post-mastectomy Pain Syndrome

Evaluation and Re-evaluation of Post-mastectomy Pain Syndrome by Breast Cancer EDGE Task Force Outcomes

Start date: March 3, 2021
Phase: N/A
Study type: Interventional

The purpose of the Breast Cancer EDGE Task Force is to provide physiotherapists with a comprehensive list of outcome measures that can be administered to a selected patient population, to assess post-mastectomy pain syndrome.

NCT ID: NCT05201963 Recruiting - Breast Cancer Clinical Trials

Erector Spinae Plane Block Versus Serratus Anterior Block on Post Mastectomy Pain Syndrome

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

Breast cancer is the most common malignancy among females. Nearly 40-60% of breast surgery patients experience severe acute postoperative pain, with severe pain persisting for 6-12 months in almost 20-50% of patients (post mastectomy pain syndrome) which is defined according to International Association for the Study of Pain (IASP) as pain which persists more than 3 months after mastectomy/lumpectomy affecting the anterior thorax, axilla, and/or medial upper arm. Regionale anesthesia is one of the strategies with the potential to prevent the development of chronic pain following breast surgery. We hypothesize that erector spinae plane block is going to be more effective than serratus anterior plane block in the prevention of postmastectomy pain syndrome.

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: NCT04874038 Recruiting - Breast Cancer Clinical Trials

Prevention of Persistent Pain With LidocAine iNfusions in Breast Cancer Surgery (PLAN)

Start date: September 22, 2021
Phase: Phase 3
Study type: Interventional

Phase III, international multicentre, parallel group, blinded, 1:1 randomized controlled trial to determine the effect of an intraoperative intravenous lidocaine infusion on reducing the development of persistent pain 3-months after breast cancer surgery.

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.