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Postoperative Pain clinical trials

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NCT ID: NCT03763760 Completed - Chronic Pain Clinical Trials

High-Dose Steroid for Hip Arthroplasty Patients Expected to Have Postoperative Pain

Start date: January 29, 2019
Phase: Phase 4
Study type: Interventional

The purpose of the Study is to test a higher dose of steroids(Dexamethasone) given just prior to surgery in the setting of Fast-Track Hip-surgery with Arthroplasty in a group of expected High Pain Responders and the effect on postoperative pain and postoperative inflammation.

NCT ID: NCT03763734 Completed - Chronic Pain Clinical Trials

High-Dose Steroid for Knee Arthroplasty Patients Expected to Have Postoperative Pain

Start date: January 29, 2019
Phase: Phase 4
Study type: Interventional

The purpose of the Study is to test a higher dose of steroids(Dexamethasone) given just prior to surgery in the setting of Fast-Track Knee surgery with Arthroplasty in a group of expected High Pain Responders and the effect on postoperative pain and postoperative inflammation.

NCT ID: NCT03758170 Completed - Surgery Clinical Trials

High-Dose Steroid for Knee Arthroplasty

Start date: January 29, 2019
Phase: Phase 4
Study type: Interventional

The purpose of the Study is to test a higher dose of steroids(Dexamethasone) given just prior to surgery in the setting of Fast-Track Kneesurgery with Arthroplasty and the effect on postoperative pain and postoperative inflammation.

NCT ID: NCT03756987 Completed - Postoperative Pain Clinical Trials

Does ESPB Improve Postoperative Quality of Recovery After VATS

Start date: December 28, 2018
Phase: N/A
Study type: Interventional

Video-Assisted Thoracoscopic Surgery (VATS) is a minimally invasive surgery. Despite reduced surgical trauma compared to the traditional thoracotomy approach, pain control after VATS remains challenging. Regional analgesia may be a crucial component of multimodal postoperative pain management. The use of nerve blocks, such as the recently described erector spinae plane block (ESPB) has been shown in case reports to reduce pain and thus has the potential to improve patient recovery. This study aims to test the hypothesis that ultrasound-guided SPB would improve the quality of recovery after VATS by reducing acute postsurgical pain.

NCT ID: NCT03751540 Completed - Postoperative Pain Clinical Trials

Retrospective Evaluation of Plane Blocks in Laparoscopic Cholecystectomy

Start date: May 1, 2018
Phase:
Study type: Observational

the investigators use usually a plane block for postoperative analgesia; if it suitable. İn laparoscopic patients; investigators used oblique subcostal transversus abdominis plane block; formerly. But in the last few months, the investigators have performed serratus intercostal (BRILMA) block with bilateral rectus sheath block. in this retrospective evaluation, the aim of the retrospective evaluation is to determine the effects of two block on postoperative opioid consumption.

NCT ID: NCT03750773 Withdrawn - Postoperative Pain Clinical Trials

Gabapentin for Relief of Immediate Postoperative Pain

GRIPP
Start date: July 2, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to use gabapentin as an additional or alternative treatment for short term pain control following cesarean delivery in order to reduce the use of opioid pain medication and improve overall pain control following surgery.

NCT ID: NCT03749395 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Erector Spinae Block for Postoperative Analgesia in Thoracotomy Patients

Start date: December 5, 2018
Phase: N/A
Study type: Interventional

aim of this study is to assess and compare between the efficacy of the new U/S guided erector spinae plane block (ESP) and the conventional methods of systemic analgesics in adult patients scheduled for elective thoracotomy surgery.

NCT ID: NCT03748498 Completed - Postoperative Pain Clinical Trials

Effect of Low Level Laser Therapy on Post-endodontic Pain

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

This study was designed as a randomized, placebo-controlled trial of 2 groups. The treatment procedures were performed by one operator. After local anesthesia and rubber dam isolation, access cavity preparation was performed by diamond burs with high-speed hand pieces under the water cooling. . Instrumentation of procedures was performed by Reciproc R50 files. Irrigation protocol was completed, canal were dried, filled with gutta-percha cones and AH Plus sealer. After chemo- mechanical instrumentation and root canal filling procedures, LLLT was applied for 60 second per tooth using Nd-YAG laser ( λ=1064 nm,100 mJ, 10 Hz, 1-W) The same procedures as in the laser group were performed, been completed but the laser was not activated in this group. These patients were assigned as placebo group. Postoperative pain was measured and documented via the Visual Analogue Scale. Chi-square test was performed in analysis of the nominal data.There was statistically significant difference between groups at the 12th and 24th hours (p<.05). ). However, no statistically significant difference was found between the groups at the 4th, 8th, 48th, and 72th hours (p>.05). No statistically significant differences were detected between the groups in terms of demographic data (age and tooth number) except for gender (P > .05).LLLT can decrease postoperative pain after root canal treatment of single rooted teeth.

NCT ID: NCT03745105 Not yet recruiting - Postoperative Pain Clinical Trials

Comparative Evaluation of the Effect of Prophylactic Intraligamentary Injection of Dexamethasone and Piroxicam on Postoperative Pain in Teeth With Symptomatic Irreversible Pulpitis

Start date: December 25, 2018
Phase: N/A
Study type: Interventional

the study is conducted to assess and compare the efficacy of local intraligamentary injection of glucocorticoids(dexamethasone) and NSAID(piroxicam) on reduction of postoperative pain in patients with symptomatic irreversible pulpitis.

NCT ID: NCT03744689 Completed - Postoperative Pain Clinical Trials

Erector Spinae Plane Block For Lumbar Disc Hernia Repair

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

Pain management after lomber disc hernia repair surgery is a challenging issue for anesthetists. Erector Spinae plane block is a novel analgesic technique which could be used for this purpose. Primary aim of this double blinded randomized controlled study is to compare the analgesic efficacy of this new block technique with control group in this group of patients.