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Pain, Postoperative clinical trials

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NCT ID: NCT05920265 Completed - Post Operative Pain Clinical Trials

Quadratus Lumborum Plain Block Versus Fascia Iliac Block

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

evaluation the efficacy of Quadratus Lumborum plain Block Versus Fascia Iliac Block for postoperative pain after hip surgery

NCT ID: NCT05919173 Completed - Post Operative Pain Clinical Trials

Comparison Between Bupivacaine and Bupivacaine With Dexmedetomidine in Caudal Block for Post Operative Pain Control

Start date: July 10, 2021
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the duration of analgesia, sedation, and intra and postoperative hemodynamics. This drug is recently available in Pakistan. To the best of our knowledge, no published data is available in this respect in Pakistan, so this study would in turn help to fill the gap in knowledge in low-resource settings/emerging economy.

NCT ID: NCT05918796 Completed - Post Operative Pain Clinical Trials

Comparison Between Bupivacaine and Bupivacaine- Dexamethasone QLB for Postoperative Analgesia

Start date: June 15, 2023
Phase: Phase 1
Study type: Interventional

The objective of this study is to assess the analgesic sparing effect of adding Dexamethasone to Bupivacaine in Quadratus lumborum block in patients undergoing Laparoscopic cholecystectomy under general anesthesia.

NCT ID: NCT05915650 Completed - Pain Clinical Trials

Application of PNE in Postoperative Pain Management of Patients With Primary Total Knee Arthroplasty

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

This study intends to carry out pain neuroscience education intervention for TKA patients to clarify the effect of this method on the degree of postoperative pain, the incidence of pain catastrophizing, kinesiophobia, and knee joint function rehabilitation in TKA patients, so as to provide a basis for clinical nursing of such patients.

NCT ID: NCT05907993 Completed - Pain, Postoperative Clinical Trials

Ibuprofen Versus Ketorolac For Postoperative Pain Relief After Cesarean Section

Start date: February 1, 2023
Phase: Phase 4
Study type: Interventional

The aim of this study will be to evaluate the effectiveness of intravenous ibuprofen versus intravenous ketorolac for postoperative pain relief after caesarian section 1. The Primary outcome is measurement of visual analogue score during rest and movement 2. The Secondary outcome is measurement of 24 hours opioids requirements.

NCT ID: NCT05904873 Completed - Pain Threshold Clinical Trials

Cold Press Test and Post Operative Pain Relationship

Start date: May 7, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate whether it is possible to get a preliminary idea about the postoperative pain in the patient with the results of a practical cold press test applied to American Society of Anesthesiologists(ASA) 1 and 2, healthy, male patients aged 16-35 before extraction of the lower third molar. The main question it aims to answer are: • Can post-operative pain be predicted with an cold test that can be applied more practically than conventional quantitative sensory tests applied preoperatively? Participants will need to keep their hands on ice for 240 seconds prior to third molar surgery. When they take their hands off the ice, they will be asked to describe their pain on the visual analog scale. After the operation, the participants are required to mark whether they use painkillers every 8 hours in their pain follow-up forms and the pain they feel according to the visual analog scale. Depending on the endurance time of the participants to keep their hands on the ice; Two different groups were determined as less than 240 sec and equal to 240 sec. The pain scores and the amount of painkiller use between these two groups were compared with each other.

NCT ID: NCT05904184 Completed - Pain, Postoperative Clinical Trials

Comparison of Calcium Silicate-based Sealer and Epoxy Resin-based Sealer

Start date: June 1, 2020
Phase: Phase 3
Study type: Interventional

Background: Sealers have been concerned with obturation. However, studies for assessing the effectiveness of endodontic treatment of sealer based on Calcium Silicate have been not much. Objective: This study aimed to assess the effectiveness of endodontic treatment of sealer based on Calcium Silicate Methods: A prospective, single-blind, clinical trial was conducted from June 2020 to December 2020 with 42 irreversible pulpitis teeth by one clinician. The postoperative pain was assessed after root canal treatment using sealer based on Calcium Silicate and sealer based on Epoxy resin after 6 hours, 12 hours, 24 hours, 48 hours, 72 hours and 7 days and inconvenient symptoms were assessed after 7 days, 3 months and 6 months. t-test, Mann-Whitney and Wilcoxon analysis were applied. Key words: obturation, sealer based on Calcium Silicate and sealer based on Epoxy resin

NCT ID: NCT05902052 Completed - Pain, Postoperative Clinical Trials

Development of Open Heart Surgery Patient Care Protocol and Its Effect on Post-sternotomy Pain

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

Open heart surgery method is generally used in the treatment of cardiovascular diseases. Sternotomy is the process of opening the sternum. After sternotomy, individuals experience ongoing pain in the anterior thorax. Despite developing pain methods and treatments, individuals undergoing cardiovascular surgery suffer from pain that cannot be managed well. Patients undergoing cardiac surgery experience severe pain for the first 48 hours and are in intensive care during this period. Pain is the most important stress factor for intensive care patients. The nurse and health care team should play a key role and take an active role in the management and evaluation of pain. However, there are not enough studies trying to define the role of the nurse in the management of postoperative pain. Protocols are used to provide pain management and routine pain assessment in intensive care units. The use of protocols provides maximum care to the patient, while reducing the cost. It also ensures the patient's participation in the treatment. While protocols ensure that practices are converted into evidence-based ones, they also prevent disruptions in treatment. As a result, management of the pain experiences of patients with sternotomy who underwent open heart surgery in the intensive care unit with the developed protocol; It will guide the improvement and development of pain management. It is thought that the protocol will address the pain of individuals undergoing open heart surgery in a holistic way. In addition, no study has been found in the literature that includes the development of a protocol for the pain of intensive care patients undergoing open heart surgery. For this reason, it is thought that the study will shed light on the literature by being a resource in the management and improvement of pain.

NCT ID: NCT05901129 Completed - Post Operative Pain Clinical Trials

The Efficacy of SPSIPB on Postoperative Pain in Patients Undergoing Shoulder Surgery

Start date: March 29, 2023
Phase: N/A
Study type: Interventional

Aim is to assess the postoperative analgesic efficacy of SPSIPB and its effect on opioid consumption in patients undergoing shoulder surgery.

NCT ID: NCT05901116 Completed - Post Operative Pain Clinical Trials

The Efficacy of SPSIPB on Postoperative Pain in Patients Undergoing Reduction Mammoplasty Surgery: Case Series

Start date: May 18, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the postoperative analgesic efficacy of SPSIPB and its effect on opioid consumption in patients undergoing reduction mammoplasty.