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Pain, Postoperative clinical trials

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NCT ID: NCT06183528 Recruiting - Analgesia Clinical Trials

Effects of Pericapsular Nerve Group Block on Postoperative Recovery for Total Hip Arthroplasty

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

The hypothesis of this study is that patients who undergo PENG block in before Total Hip Artroplasthy (THA) surgery with spinal anesthesia will have reduced postoperative pain scores, less need for opioid analgesics and earlier mobilisation.

NCT ID: NCT06183073 Recruiting - Postoperative Pain Clinical Trials

Caudal Block With Bupivacaine and Dexmedetomidine Versus TAP Block With Bupivacaine Alone for Postoperative Analgesia in Pediatric Undergoing Infraumbical Surgeries

Start date: April 2, 2023
Phase: Phase 2
Study type: Interventional

Acute pain management for pediatric surgical patients intraoperatively and postoperatively is important for their comfort and psychological impact. Children aged 3-9 years old are included in the study and are divided randomly into two groups (45 children in each): Group D: Caudal block with bupivacaine 0.25% in a dose of (1 ml / kg) and dexmedetomidine 1μg/ kg. Group T: TAP block with bupivacaine 0.25% in a dose of (0.5 ml / kg).

NCT ID: NCT06183021 Recruiting - Pain, Postoperative Clinical Trials

The Effect of Cryotherapy on the Outcome of Pulpotomy and Root Canal Treatment

Start date: December 13, 2023
Phase: N/A
Study type: Interventional

The goal of this randomized clinical trial is to compare the outcome of total amputation and root canal treatment with or without cryotherapy in terms of postoperative pain, quality of life, and treatment success for the management of deep dentinal caries. The main questions it aims to answer are: Does cryotherapy influence the outcome, life quality and treatment success in total pulpotomy? Does cryotherapy influence the outcome, life quality and treatment success in root canal treatment? Does the outcome of total pulpotomy and root canal treatment differ in cases of pulpitis? There are 4 experimental groups: 1. Total pulpotomy with cryotherapy group 2. Total pulpotomy group (Control 1) 3. Root canal treatment with cryotherapy group 4. Root canal treatment group (Control 2)

NCT ID: NCT06182111 Not yet recruiting - Postoperative Pain Clinical Trials

Intraoperative Administration of Intravenous Morphine in Patients Undergoing Laparoscopic Cholecystectomy

MORPHLAPCHOL
Start date: February 2024
Phase:
Study type: Observational

The goal of this observational, quality improvement study is to compare the effect of a dose of morphine given during gall-bladder removal surgery. The main questions to answer are: - Do participants, who are given given a dose of morphine during gall-bladder removal surgery, experience less pain after surgery? - Does a dose of morphine during gall-bladder removal surgery cause more side effects? The investigators will compare the effects of two types of anesthesia: a) anesthesia without morphine during surgery, and b) anesthesia with morphine during surgery.

NCT ID: NCT06182059 Recruiting - Knee Arthropathy Clinical Trials

Persistent Post Surgical Pain After Total Knee Arthroplasty

Start date: January 12, 2024
Phase: N/A
Study type: Interventional

Patients undergone total knee replacement are randomized to receive a "fast track" regional anesthesia protocol or a "traditional" regional anesthesia continuous infusion by both a femoral and sciatic catheter to assess if this latter technique may reduce persistent postoperative pain six months after surgery

NCT ID: NCT06179641 Recruiting - Postoperative Pain Clinical Trials

Comparison of Two Different Regional Analgesia Techniques for Patients Undergoing Total Knee Arthroplasty

PIPACK
Start date: February 8, 2024
Phase: N/A
Study type: Interventional

The objective of this clinical trial is to compare two regional analgesia techniques in patients undergoing total knee arthroplasty: IPACK (Infiltration of local anesthetic between the Popliteal Artery and Capsule of the Knee) vs selective tibial nerve block. The main question is whether one of these peripheral blocks is more effective in reducing postoperative pain than the other. All patients will have a spinal block with an adductor canal block. One group will receive an IPACK block and the other group, a selective tibial nerve block. Postoperative pain scores and morphine consumption, among others, will be compared between groups.

NCT ID: NCT06177665 Recruiting - Postoperative Pain Clinical Trials

Comparison of Erector Spina Plan Block and Rhombodid Intercostal Block in Breast Surgery

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

In this study, the investigators compared ultrasound-guided erector spinae plane (ESP) block and rhomboid intercostal block (RIB) on postoperative analgesic effect in unilateral breast surgery.

NCT ID: NCT06177652 Recruiting - Postoperative Pain Clinical Trials

Postoperative Analgesis for Pain Management After Thoracotomy

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Thoracotomy is among the most painful surgical procedures and can cause severe pain. Postoperative pain causes many complications. Therefore, pain management is important in patients undergoing thoracotomy. For this purpose, systemic analgesics are used along with ultrasound-guided nerve blocks in thoracotomy pain. The effectiveness of thoracic paravertebral block and serratus plane block in the treatment of post-thoracotomy pain will be evaluated by comparing their effectiveness and complications on postoperative pain. Since the epidural spread of the thoracic paravertebral block is more effective, the effectiveness of postoperative pain relief will be more effective

NCT ID: NCT06176222 Not yet recruiting - Clinical trials for Postoperative Complications

Combined Use of Naldebain® ER Injection and Precedex® After VATS

Start date: December 28, 2023
Phase: Phase 4
Study type: Interventional

The goal of this clinical trial is to investigate the effects of combined use of Naldebain® ER Injection and Precedex® in patients received video-assisted thoracoscopic surgery. The main questions it aims to answer are: - the pain intensity after surgery - the level of dizziness after surgery Participants will receice ultrasound-guided thoracic paravertebral nerve block, intramuscular Naldebain® ER injection and intravenous Precedex® infusion. If there is a comparison group: Researchers will compare experimental group with placebo group to see if pain and dizziness after surgery can reduced.

NCT ID: NCT06172465 Recruiting - Analgesia Clinical Trials

Comparison of OSTAP and EOIP Blocks in Laparoscopic Cholecystectomies

Start date: January 5, 2024
Phase: N/A
Study type: Interventional

Laparoscopic cholecystectomy (LC) surgery causes postoperative severe pain. As part of multimodal analgesia aimed at reducing postoperative opioid consumption and providing effective analgesia, ultrasound (US)-guided transversus abdominis plane block (TAP) and external oblique intercostal plane block (EOIPB) will be applied as regional anesthesia methods. There is no study in the literature comparing OSTAP and EOIP blocks, and our goal is to evaluate the analgesic effectiveness between OSTAP and EOIP blocks in LC surgeries.