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Pain, Postoperative clinical trials

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NCT ID: NCT05796778 Recruiting - Post Operative Pain Clinical Trials

Sub Omohyoid Suprascapular Nerve Block Versus Interscalene Nerve Block

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

Shoulder surgery can be very painful surgery after which the use of opioids is often required. The well-known side-effects of opioids (e.g. respiratory depression, somnolence, nausea, vomiting, and pruritus) limit their use in so called 'fast track' surgery and anaesthesia programmes. the study aimed to compare the effect of sub omohyoid suprascapular nerve block versus interscalene nerve block in preventing postoperative pain and decreasing analgesic consumption in patients scheduled for shoulder surgery

NCT ID: NCT05795413 Recruiting - Post Operative Pain Clinical Trials

Quality of Recovery From Mastectomy With and Without PECS Blocks

Start date: April 25, 2023
Phase:
Study type: Observational

This is a prospective observational study. Investigators want to understand post-operative recovery for patients undergoing mastectomy at NorthShore University HealthSystem. Some of these patients receive PECS blocks with Liposomal Bupivacaine and some do not receive a block. Investigators want to know whether patients who receive a block have better post operative recovery and pain control than patients who do not receive one. Investigators also want to understand whether PECS blocks with Liposomal Bupivacaine improves quality of recovery at 72 hours post operatively.

NCT ID: NCT05792124 Recruiting - Postoperative Pain Clinical Trials

Comparison of the Effects of Retro Laminar Block (RLB) and Erector Spina Area Block (ESP) on Postoperative Recovery Quality and Pain in Lumbar Spinal Surgery

Start date: January 31, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare the efficacy of erector spinae plane block (ESPB) and Retrolaminar Block on postoperative recovary quality and pain after lumbar spinal surgery

NCT ID: NCT05787691 Recruiting - Clinical trials for Chronic Post Surgical Pain

Enhanced vs.Standard Pain Management of Patients at Risk for Chronic Post-surgical Pain

ALDOpilot
Start date: May 12, 2023
Phase: N/A
Study type: Interventional

The goal of this pragmatic pilot clinical trial is to test the feasibility of the trial in terms of the number of patients recruited in a given period. The main question it aims to answer is to assess the number of eligible patients and number of patients willing to participate per month. Participants will be followed either by the team of "transitional pain service" (intervention group) or by a surgeon or the general practitioner (standard care). Depending on individual risk factors, patients in the intervention group will be offered some targeted measures, for example: - hypnosis, - patient education, - evaluation by psychiatrist, - psychotherapy, - locoregional anesthesia, - anti-depressant treatment Participants (in both intervention and standard care groups) will be asked to answer some questions before surgery, during the first week following the surgery and six months after the surgery.

NCT ID: NCT05785572 Recruiting - Post Operative Pain Clinical Trials

Effect of Radiofrequency of Suprascapular Nerve in Shoulder Reverse Arthroplasty

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

The purpuse of this study is to asses if the pulsed radiofrecuency of the supraescapular nerve and accesory nerve have the same or superior efectivity controlling the acute postoperative pain than interscalenic braquial plexus block

NCT ID: NCT05785234 Recruiting - Stomach Neoplasms Clinical Trials

The Effects of Sufentanil vs. Remifentanil in Total Intravenous Anesthesia With Remimazolam on Postoperative Pain

Start date: April 2023
Phase: N/A
Study type: Interventional

In this study, the investigators evaluate the effect of total intravenous anesthesia using sufentanil-remimazolam and remifentanil-remimazolam on postoperative pain in patients undergoing laparoscopic gastrectomy.

NCT ID: NCT05783440 Recruiting - Pain Clinical Trials

Direct Patient Feedback on Postoperative Pain

DPF
Start date: July 6, 2022
Phase: N/A
Study type: Interventional

Postoperative pain is common, can be severe, has a negative impact on outcomes after surgery and brings along major economic costs for society. A substantial part of patients may develop persistent post-surgical pain. Severity and duration of pain after surgery appear to have a role in this process but the transition from acute postoperative pain to chronic pain is only partially understood. Effective treatment of postoperative pain is hampered by several barriers, including the way measurement of pain and registration of pain-scores are carried out by nurses in clinical practice. Modern technology offers new opportunities for pain measurement and direct patient feedback on postoperative pain, during and also after clinical admission. We developed a smartphone application that allows clinical patients to report pain scores and other pain related outcomes on postoperative pain with their own telephone device. Patient reported pain scores > 3 on a Numeric Rating Scale (NRS) 0-10 are immediately passed on to the nurse who receives a message of the reported pain score. This can lead to earlier detection of pain and a more timely treatment resulting in improved patient reported outcomes on postoperative pain

NCT ID: NCT05780333 Recruiting - Post Operative Pain Clinical Trials

Effect of Different Plane Blocks on Quality of Recovery and Postoperative Pain After Laparoscopic Hysterectomy

Start date: January 27, 2023
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to evaluate in effect of tap block and esp block on quality of recovery and postoperative pain after laparoscopic hysterectomy. The main question it aims to answer are: Are these two plane blocks used superior to each other? Participants; - will fill out the preoperative questionnaire - will fill out the postoperative questionnaire - will report their pain status according to the NRS score

NCT ID: NCT05775861 Recruiting - Anesthesia Clinical Trials

Dexmedetomidine Added to Ropivacaine Single Shot vs Continuous Interscalene Nerve Block

DEXBIB
Start date: August 23, 2022
Phase: N/A
Study type: Interventional

Arthroscopic shoulder surgery is increasingly performed in an outpatient setting and post-operative pain management is often a real challenge as those surgeries are well recognized for their high level of pain which often affects physical rehabilitation. The interscalene block is a largely used anesthetic technique to perform these surgeries whilst avoiding general anesthesia (GA) and to provide postoperative analgesia. However, the painful period often exceeds the duration of a single shot block, thus affecting patient recovery. Some specialized centers use a continuous catheter and elastomeric pump in order to prolong the duration of analgesia. However, several logistical, professional and financial constraints limit the use of these catheters and pumps in a great number of outpatient centers. On the other hand, perineural dexmedetomidine is increasingly used as an adjuvant to improve block onset, analgesia duration and patient satisfaction. The use of adjuvants such as perineural dexmedetomidine added to a single shot interscalene block appears to be an interesting option to prolong postoperative analgesia without the limitations imposed by a continuous catheter and elastomeric pumps in arthroscopic shoulder surgeries.

NCT ID: NCT05775393 Recruiting - Post Operative Pain Clinical Trials

Effects of Adding Dexamethasone Plus Ketamine to Bupivacine in Serrtatus Plane Block

Start date: February 20, 2022
Phase: N/A
Study type: Interventional

This randomized, double-blind trial included 60 female patients undergoing modified radical mastectomy. The study carried out at National Cancer Institute, cairo university after approval of the local ethical committee. The study aiming to compare the analgesic efficiency of adding dexamethasone or ketamine plus dexamethasone to bupivacaine in ultrasound-guided serratus anterior plane block (SAPB) performed with modified radical mastectomy surgery.