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Pain, Postoperative clinical trials

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NCT ID: NCT04213716 Completed - Pain Clinical Trials

Comparison of the Efficacy of Calcium Hydroxide With Silver Nanoparticle and Conventional Calcium Hydroxide Intra Canal Medications on Post-Operative Pain in Symptomatic Root Canal Treatment Failure Cases:

CSNIMSRRT
Start date: June 15, 2015
Phase: Phase 2
Study type: Interventional

The aim of this study is to measure and compare the effectiveness of nanosilver combined calcium hydroxide and conventional calcium hydroxide intracanal medications in reducing postoperative pain in patients with Symptomatic Root Canal treatment Failure .

NCT ID: NCT04209907 Completed - Postoperative Pain Clinical Trials

the Effect of Retrolaminar Block on Postoperative Pain

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

In recent years, as a part of multimodal analgesia, paravertebral blocks are replacing epidural analgesia due to the less side effects. Although the risk of pneumothorax is the most feared complication in paravertebral blocks, retrolaminar block (RLB) -which is a paravertebral block- significantly reduces this risk due to the anatomical technique of procedure. The investigators aim to investigate the effect of retrolaminar block with ultrasound- guided on perioperative analgesia for patients undergoing lumbar vertebra surgery.

NCT ID: NCT04209764 Completed - Pain, Postoperative Clinical Trials

Prevalence of Pain in the Departments of Surgery and Oncoematology of a Children's Hospital

Start date: November 6, 2022
Phase:
Study type: Observational

Six years after, the authors will conduct the same analysis to check if there have been any improvements in the management of analgesic therapy after the measures taken according to the results of the previous study conducted in the same departments. During a single day work three committees, administering a questionnaire to patients or parents, will evaluate the adherence to international recommendations (JCI and WHO) in the management of analgesic therapy.

NCT ID: NCT04209478 Completed - Pain, Postoperative Clinical Trials

Transversus Abdominis Plane Block and Quadratus Lumborum Block in Pediatric Patients

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

In the pediatric age group, postoperative pain is very important for the children to have a comfortable and problem-free postoperative period. In the present study, it was aimed to compare the postoperative analgesic efficacy of Transversus abdominis plane (TAP) Block, and quadratus lumborum block (QLB) Type 1 on the pediatric patients

NCT ID: NCT04208568 Completed - Cholelithiasis Clinical Trials

Comparison of Postoperative Pain After Gallbladder Retrieval From Umbilical and Epigastric Ports.

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

To know the association of postoperative pain after gallbladder removal from umbilical port site versus epigastric portsite, after four ports laparoscopic cholecystectomy,and the epigastric port site was found to be friendly for the patients in terms of less pain after gallbladder removal from this site after surgery.

NCT ID: NCT04205695 Completed - Anesthesia Clinical Trials

Comparison of Catheters Orifice Configuration For Continuous Infraclavicular Analgesia

Start date: December 10, 2019
Phase: N/A
Study type: Interventional

Infraclavicular nerve catheter for postoperative analgesia will be included in the 70 adult patients undergoing upper extremity surgery included in the study. These patients will be randomized to the catheter tip configuration as CEMP (closed-ended multiport catheter) group and OESP (open-ended single port catheter) group. Patient controlled analgesia device will be attached to the peripheral nerve catheter of these patients. Demographic data of the number of pushing the button, the amount of bolus dose given, the total dose given in the patient controlled anesthesia device, the need for additional analgesia and the amount, pain scores, complications will be recorded for three days postoperatively. Records will be compared statistically.

NCT ID: NCT04203537 Completed - Postsurgical Pain Clinical Trials

Study Evaluating the Safety, Efficacy and Pharmacokinetics of CA-008 (Vocacapsaicin)

Start date: December 4, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

In the pilot (Part A) of this study, multiple doses of CA-008 (vocacapsaicin) were evaluated for safety, tolerability, and PK. Doses were then selected for the expanded part (Part B) of the study, where CA-008 was compared to placebo. Patients had serial assessments of safety, PK, and drug effect.

NCT ID: NCT04202250 Completed - Anesthesia Clinical Trials

The Efficacy of Continuous Femoral Nerve Catheter Orifice Configuration for Postoperative Analgesia in Knee Arthroplasty

Start date: December 10, 2019
Phase: N/A
Study type: Interventional

Femoral nerve catheter for postoperative analgesia will be included in the adult patients undergoing total knee arthroplasty included in the study. These patients will be randomized to the catheter tip configuration as CEMP (closed-ended multiport catheter) group and OESP (open-ended single port catheter) group. Patient controlled analgesia device will be attached to the peripheral nerve catheter of these patients. Demographic data of the patients , the number of pushing the button the amount of bolus dose given, and the total dose given in the patient controlled anesthesia device, the need for additional analgesia and the amount, pain scores, complications will be recorded for three days postoperatively. Records will be compared statistically.

NCT ID: NCT04197531 Completed - Post Operative Pain Clinical Trials

Postoperative Pain After the Use of Different Last Irrigation Method During Root Canal Treatment in Primary Teeth

Start date: April 1, 2018
Phase: N/A
Study type: Interventional

This study was to evaluate and compare the postoperative pain levels after using EndoActivator and conventional endodontic syringe irrigation in root canal therapy of primary molars.

NCT ID: NCT04197206 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Costotransverse Block for Breast Cancer Surgery

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

Costotransverse block is a novel regional anesthesia technique described a few months ago. It's use for breast surgery has been reported by only one case report in the literature. As the investigators have considered that Costotransverse block can be efficacious for providing postoperative analgesia in the breast surgeries, the investigators have implemented the application of this blockade into practice at the clinic. The main purpose of this study is to evaluate the analgesic effect of ultrasound-guided unilateral costotransverse block in breast cancer surgery.