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Pain, Postoperative clinical trials

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NCT ID: NCT05004636 Completed - Clinical trials for Post-operative Pain, Acute

Adductor Canal Blocks With Bupivacaine and Magnesium After Same-day Discharge Total Knee Arthroplasty Improve Post-operative Pain Relief and Decrease Opioid Consumption: a Prospective Randomized Controlled Trial

Start date: August 5, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the addition of magnesium to bupivacaine for the post-operative adductor canal blocks (ACB) can decrease opioid consumption and improve pain management for patients after same-day discharge total knee arthroplasty (TKA). The investigators will assess whether the addition of magnesium will decrease visual analog scale (VAS) pain scores, decrease post-operative total opioid consumption (oral morphine equivalents), decrease the incidence of post-operative nausea and vomiting (PONV), and improve patient satisfaction in comparison to when magnesium is not administered.

NCT ID: NCT05004532 Completed - Postoperative Pain Clinical Trials

Transversus Abdominis Plane Block in Acute Appendicitis Pain Managment

Start date: January 1, 2017
Phase:
Study type: Observational

In this study, it was aimed to investigate the analgesic efficacy of the preoperatively applied Transversus Abdominis Plane (TAP) Block in the management of acute appendicitis-related abdominal pain and post-appendectomy pain.

NCT ID: NCT05004506 Active, not recruiting - Clinical trials for Post-Operative Pain, Chronic

Intra-articular Analgesia Versus Adductor Canal Block for Arthroscopic Knee Surgery

Start date: April 20, 2016
Phase: Phase 3
Study type: Interventional

This study is a randomized study that compares two commonly used post-operative pain reducing techniques by measuring the level of pain and use of pain medication after knee surgery.

NCT ID: NCT05003765 Recruiting - Clinical trials for Post-operative Pain Management

Are Superficial Parasternal Intercostal Plane (SPIP) Blocks With Bupivacaine and With or Without Adjuvants Helpful for Post-operative Pain After Coronary Artery Bypass Grafting?

Start date: August 6, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the addition of the superficial parasternal intercostal plane (SPIP) block alone (30cc of 0.25% bupivacaine) or plus Magnesium (200mg of magnesium sulfate) or plus Magnesium + Buprenorphine (300mcg) as adjuvants can improve post-operative pain in patients undergoing cardiothoracic surgery, specifically, coronary artery bypass grafting (CABG)

NCT ID: NCT04999670 Not yet recruiting - Pregnancy Related Clinical Trials

Fascial Closure and Post-caesarean Pain

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

This study will evaluate post-operative pain in patients undergoing elective caesarean sections based on the method of fascial closure. Patients will be randomised into one of three groups based upon the method of fascial closure and will be followed up over a 10 week period evaluating analgesia use in the acute setting, and also following up with pain scores using a visual analogue score throughout the follow-up period.

NCT ID: NCT04999319 Completed - Postoperative Pain Clinical Trials

Morphine Consumption in Thoracotomy

Start date: October 15, 2020
Phase: N/A
Study type: Interventional

Importance of effective postoperative pain management is well known. The undesired effects of pain can be prevented with multimodal analgesia for the patient. Thoracotomy operations are associated with high levels of pain. With the use of ultrasound, many regional anesthesia techniques were described to provide effective postoperative analgesia. The aim of this study was to compare the postoperative effect of paravertebral block (PVB) and erector spinal plane block (ESPB) in thoracotomies.

NCT ID: NCT04998071 Recruiting - Postoperative Pain Clinical Trials

Posterior Quadratus Lumborum Block Using 0.125% Versus 0.25% Bupivacaine for Analgesia in Children Undergoing LPEC

Start date: August 15, 2021
Phase: N/A
Study type: Interventional

The aim of the present study is to evaluate and compare the analgesic efficiency of the difference concentration between 0.125% and 0.25% bupivacaine provided by ultrasound guided posterior quadratus lumborum block undergoing LPEC in children

NCT ID: NCT04997174 Recruiting - Postoperative Pain Clinical Trials

Comparison of Postoperative Pain Management in Patients Undergoing Laparoscopic Colorectal Surgery Under Enhanced Recovery After Surgery (ERAS) Program, Laparoscopic Colorectal Surgery Without ERAS and Open Colorectal Surgery

Start date: October 2021
Phase:
Study type: Observational

This is a retrospective study to compare postoperative pain intensity in patients going laparoscopic colorectal surgery with Enhanced Recovery after Surgery (ERAS), without ERAS and open colorectal surgery.

NCT ID: NCT04996290 Completed - Pain, Postoperative Clinical Trials

Combined PENG and LFCN Block for Total Hip Arthroplasty

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

A clinical trial investigating the effect of a combined locoregional anesthesia technique on the postoperative analgesia outcomes after a total hip arthroplasty. A PENG block will be used in combination with a LFCN block. The results will be compared to a control group that is solely treated with intravenous analgesia. This technique aims to provide improved pain scores after surgery without interference of revalidation.

NCT ID: NCT04996251 Completed - Pain, Postoperative Clinical Trials

Pre-incision Versus Post-incision Local Anesthetic During Robotic Sacrocolpopexy

CLAPPS
Start date: July 30, 2021
Phase: Phase 4
Study type: Interventional

Obtaining Likest-pain scale score on postoperative day one after injection of local anesthetic into incision sites of a laparoscopic/robotic-assisted sacrocolpopexy