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Regional Anesthesia clinical trials

View clinical trials related to Regional Anesthesia.

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NCT ID: NCT05822479 Active, not recruiting - Postoperative Pain Clinical Trials

Laparoscopic Sleeve Gastrectomy Surgery and External Oblique Intercostal Block

Start date: April 20, 2023
Phase: N/A
Study type: Interventional

In obese patients, adequate pain relief in the postoperative period is an important parameter that affects patient comfort and hospital stay. Increasing patient comfort and recovery quality can be achieved by avoiding undesirable effects such as nausea, vomiting, and analgesia. This study aimed to evaluate the impact of the external oblique intercostal block postoperative acute pain scores and opioid consumption in the first 24 hours after laparoscopic sleeve gastrectomy surgery.

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: NCT05792345 Not yet recruiting - Regional Anesthesia Clinical Trials

Comparison of Post-operative Analgesia in Pediatric Superficial TTMPB

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

When a patient is to undergo heart surgery with a sternotomy, a transthoracic block is performed. The thoracic block is an analgesic technique which consists of injecting anesthetic product into the nerves, in order to avoid significant pain. The common technique is to make injections in the sternum by the surgeon. A new, increasingly widespread method is performed by the anesthetist who performs the block under ultrasound. This research project aims to determine if performing this transthoracic block under ultrasound is more effective than injections performed by the surgeon without ultrasound.

NCT ID: NCT05783128 Recruiting - Airway Management Clinical Trials

The Effect of Different Methods of Airway Management on the Stomatognathic System: an Observational Prospective Study.

Start date: March 1, 2023
Phase:
Study type: Observational

The manipulations required during airway management and the different methods of establishing an airway (endotracheal intubation, supraglottic airway device etc) during anesthesia, as well as certain drugs used during anesthesia and sedation, may have an impact to the stomatognathic system. These effects can vary from a subtle temporomandibular joint disc displacement with reduction to the onset of temporomandibular disorders to previously healthy subjects.This observational prospective study aims at investigating the effect of different methods of airway management during anesthesia on the stomatognathic system (including temporomandibular joint, mastication muscles, occlusion etc).

NCT ID: NCT05678777 Recruiting - Regional Anesthesia Clinical Trials

Use of Galvanic Skin Response to Measure Peripheral Block Activity

Start date: January 30, 2022
Phase:
Study type: Observational

the investigators aim in this study is to determine whether the block is successful in successful infraclavicular brachial plexus blocks performed with USG, according to the change in GSR value in the upper extremity blocked due to sympathetic nerve blockade. Block success will be evaluated by sensory and motor examination of the blocked arm.

NCT ID: NCT05642975 Completed - Postoperative Pain Clinical Trials

Comparing Suprainguinal Fascia Iliaca Block With Erector Spinae Plane Block in Hip and Proximal Femur Surgery

Start date: August 1, 2022
Phase:
Study type: Observational [Patient Registry]

Most hip fractures occur in the elderly population. Opioid-related respiratory depression is more common in the elderly population but can cause severe brain damage or death. Reducing the amount of opioids administered before, during and after surgery by adding a regional block may increase the postoperative quality of recovery, reduce chronic pain syndromes, and may potentially facilitate the participation of patients in rehabilitation. Despite their potential advantages, peripheral nerve blocks are still not widely used in people with hip fractures. The primary objective of this study is to compare patients' postoperative pain scores and opioid consumption.

NCT ID: NCT05589246 Recruiting - Acute Pain Clinical Trials

Regional Analgesia in Combination With Cryoanalgesia to Prevent Acute Pain Following Nuss Procedure

Start date: September 28, 2022
Phase: N/A
Study type: Interventional

Funnel chest deformation is a painful procedure, which requires high doses and long time used of opioids. It makes difficult introduction of ERAS protocol. Intraoperative cryolesia of intercostal nerves serves great relief of pain after this procedures. However ablation of the nerves needs 12-24 hours to achieve effects. During this time the high doses of opioids are needed. It causes side effects (sedation makes rehabilitation difficult). On the other hand, percutaneus cryoablation performed 12-24 hours before Nuss procedure needs repeated general anaesthesia. The investigators hypothesed that regional analgesia (erector spine plain block) performed just before intraopertive cryolesia may cover time to full cryolesia effect.

NCT ID: NCT05578885 Not yet recruiting - Regional Anesthesia Clinical Trials

Duration of Analgesia in Bier Block for Patients Undergoing Hand Surgery

Start date: February 1, 2024
Phase: N/A
Study type: Interventional

Intravenous regional anesthesia (Bier block) is widely used as an anesthetic technique for operations of short duration of the distal upper or lower extremities Today, IVRA is still popular in many countries being used in the emergency room, for outpatients and for high-risk patients with contraindications for general anesthesia.

NCT ID: NCT05450211 Completed - Regional Anesthesia Clinical Trials

Evaluation of Postoperative Analgesic Efficacy of Suprainguinal Fascia Iliaca Block

Start date: July 25, 2022
Phase: N/A
Study type: Interventional

It was aimed to evaluate the postoperative analgesic efficacy of the suprainguinal fascia iliaca block applied in the postoperative period in terms of 24-hour opioid consumption, pain score, additional analgesic need, and side effects and complications in the postoperative period, and to see the postoperative analgesic effectiveness of this block in patients who underwent knee arthroplasty.

NCT ID: NCT05416541 Active, not recruiting - Anxiety Clinical Trials

Uncontrolled Disinformation About Regional Anesthesia and Pregnant Patients.

Start date: May 1, 2022
Phase:
Study type: Observational [Patient Registry]

Nowadays, hundreds of information about regional anesthesia are accessed from any internet search engine when a question is written about the methods of anesthesia that can be applied during C/S. This information may have positive or negative effects on the patient, as well as include uncontrolled, unsupervised comments, articles and images. Our aim is primarily to evaluate whether our patients are exchanging information via social media or the internet and the effects of these shares on their concerns.