Clinical Trials Logo

Mastectomy clinical trials

View clinical trials related to Mastectomy.

Filter by:

NCT ID: NCT04296188 Not yet recruiting - Pain, Postoperative Clinical Trials

Erector Spina Plane Block vs Serratus Anterior Plane Block for Postoperative Mastectomy Pain

Start date: March 18, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the efficiency of serratus anterior plane block and erector spina plane block on analgesic consumption, postoperative pain and patient's satisfaction and recovery quality in patients undergoing mastectomy.

NCT ID: NCT04270136 Completed - Breast Cancer Clinical Trials

Feasibility of Total Mastectomy in Ambulatory Care

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

Breast cancer is the first female cancer in France. Total mastectomy occurred in 30% of breast cancer patient population. The purpose of this study is to evaluate the feasibility of outpatient surgery for the total mastectomy. In France, Ambulatory care is developed as part of the new national health plan. Breast conserving surgery for tumorectomy or partial mastectomy is already done in outpatient vacation. Total mastectomy is an extension of this surgery, and, as such, underpins the investigator's hypothesis that total mastectomy is feasible in outpatient care .

NCT ID: NCT04108715 Completed - MASTECTOMY Clinical Trials

Erector Spina Plane Block Versus Deep Serratus Anterior Plane Block for Post Mastectomy Analgesia

Start date: July 7, 2019
Phase: N/A
Study type: Interventional

Breast cancer surgery like Mastectomy and modified radical mastectomy are associated with significant postoperative pain, and management depends largely on patient controlled analgesia with intravenous Morphine or other opioids equivalents. Respiratory depression, Ileus, sedation, nausea and vomiting are some of the potential side effect of opioid treatment which prolonged hospital length of stay and increase the coast. Recent advance in ultrasound guided regional anesthesia has led to the development of two novel regional anesthesia techniques specific to chest wall analgesia; Erector spina plain block and Serratus anterior plain block, with its potential to reduce or eliminate the need for opioids to manage post-operative pain.

NCT ID: NCT04029467 Recruiting - Breast Cancer Clinical Trials

Effect of Dexmedetomidine on the Duration of Pain Control in ESP Block for Breast Surgery

Start date: July 17, 2019
Phase: Phase 4
Study type: Interventional

Patients undergoing Partial or total mastectomy with axillary LN dissection will receive prior to induction of general anaesthesia ESP block at T4 level at the same side of the surgery. one group will receive ropivacaine 0.375% and the other will get ropivacaine 0.375% with dexmedetomidine 0.5mcg/kg as an adjuvant. time to first narcotic requirement will be documented and therefore an assessment of the duration of action of the block will be made

NCT ID: NCT04019834 Completed - Breast Cancer Clinical Trials

Preoperative Regional Nerve Block for Acute and Chronic Post-Operative Pain Following Mastectomy

RELIEF
Start date: July 6, 2020
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to see if pre-operative regional nerve blocks compared to a placebo nerve block can decrease chronic post mastectomy pain, immediate postoperative pain and postoperative narcotic consumption.

NCT ID: NCT03959709 Recruiting - Breast Cancer Clinical Trials

Pre-pectoral Versus Sub-pectoral Implant Placement in Immediate Breast Reconstruction

Start date: August 22, 2019
Phase: N/A
Study type: Interventional

Despite the popularity and proved safety of prepectoral implant-based reconstruction, there is little evidence on long-term results and variables which could influence surgical outcome. So far, no specific guidelines or indications have been developed for prepectoral technique and heterogeneous inclusion criteria had been used in previous reports. There is a lack of studies documenting outcomes following ADM-assisted prepectoral breast reconstruction, and there are no randomised controlled trial studies that drawing a direct comparison of clinical or patient-reported outcomes between subpectoral and prepectoral groups. The investigators hypothesized that immediate acellular dermal matrix-assisted implant-based breast reconstruction with prepectoral implant placement would result in less early postoperative pain but more reported implant rippling, requirement of more fat grafting and an equitable safety profile compared with ADM-assisted implant-based breast reconstruction with subpectoral implant placement. The aim of this study is to evaluate the postsurgical pain, complications and patient-reported outcomes of prepectoral breast reconstruction versus subpectoral implant placement in immediate breast reconstruction.

NCT ID: NCT03757793 Recruiting - Clinical trials for Breast Reconstruction

Near-infrared Spectroscopy for Monitoring Tissue Oxygenation in Breast Reconstruction

Start date: September 28, 2018
Phase:
Study type: Observational

The study will evaluate the use of near infrared spectrometry (NIRS)in detecting early microvascular complications in deep inferior epigastric artery perforator (DIEP)-flap(s).

NCT ID: NCT03711916 Completed - Breast Cancer Clinical Trials

Post-Operative Outcomes of Low Thermal Dissection vs. Traditional Electrosurgery

Start date: March 17, 2017
Phase: N/A
Study type: Interventional

Low thermal dissection devices have been introduced as a tool to improve surgical outcomes. PlasmaBlade, a low thermal dissection device, has shown to be associated with effective cutting, and significantly lower temperature than traditional electrosurgical dissection device. Thus, low thermal devices would improve flap perfusion by decreasing the thermal injury resulted by the dissection. Looking into the use of low thermal devices in cases of mastectomy and immediate breast reconstruction has not been documented. The aim of this study is to determine if there are clinical flap perfusion, surgical site drainage, and pain scores differences between mastectomy flaps created using low thermal dissection device and those done with the standard care of Bovie cautery in order to warrant a formal study.

NCT ID: NCT03618433 Completed - Breast Cancer Clinical Trials

KÄ°NECT® - Video Games Based Physiotherapy Programme in Patients With Breast Cancer Surgery

Start date: September 3, 2018
Phase: N/A
Study type: Interventional

The main objective of the study is to investigate the effects of Kinect® video based technology on pain, functionality, muscle strength, fatigue and quality of life in patients with breast cancer surgery and axillary node dissection.

NCT ID: NCT03614091 Recruiting - Pain, Postoperative Clinical Trials

Paravertebral Block Versus Erector Spinae Plane Block for Modified Radical Mastectomy in Womens.

Start date: February 1, 2020
Phase: N/A
Study type: Interventional

postoperative pain following Modified radical mastectomy is severe specially after dissection of tissues .paravertebral plane block provides an excellent postoperative analgesia for women's,but it carry the risk of pneumothorax which it reported in some cases.Erector spinae plane block is a recent block has been mentioned in many case reports as a safe,quick and can be used in outpatient setting. we use a comparative study to compare the postoperative analgesia between both blocks and the affection of postoperative pain following both blocks if any on pulmonary functions.