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Pain, Postoperative clinical trials

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NCT ID: NCT05823363 Recruiting - Postoperative Pain Clinical Trials

Vaginal Cuff Infiltration With Liposomal Bupivacaine for Pain Relief: A Double Blind, Randomized Controlled Trial

Start date: April 10, 2023
Phase: Phase 4
Study type: Interventional

The goal is to find out if Exparel (liposomal bupivacaine) given as an injection decreases pain score if given into the vaginal cuff right before starting the minimally invasive (robotic-assisted or laparoscopic) total hysterectomy in patients scheduled for benign indication? Participants will write down 1. pain score at various intervals 2. pain medication used Treatment patients will receive 1)intervention arm will receive Exparel mixed with bupivicaine 2)control arm will receive bupivicaine only

NCT ID: NCT05822011 Recruiting - Post Operative Pain Clinical Trials

Ultrasound Guided Rhomboid Intercostal Subserratus Plane Block vs Erector Spinae Plane Block in Open Nephrectomy

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

Our aim is to measure the efficacy of rhomboid intercostal subserratus plane block and erector spinae plane block in comparison to thoracic epidural block in patients undergoing open nephrectomy

NCT ID: NCT05821725 Recruiting - Palatal Wound Clinical Trials

Effects of Topical Hyaluronic Acid Gel on Postoperative Pain and Wound Healing

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

This clinical study aims to investigate the impact of a topical hyaluronic acid (HA) gel on postoperative pain and wound healing at palatal donor sites in patients undergoing mucogingival procedures involving a de-epithelialized gingival graft (DGG) from the palate. The study design is a Phase III, randomized, double-blind, parallel-group, clinical trial, conducted in a single center, with 30 subjects aged 18-70 years.

NCT ID: NCT05820646 Recruiting - Intervention Clinical Trials

Effect of Boswellia Sacra as an Intracanal Medicament on Postoperative Pain Intensity and Bacterial Load Reduction

Start date: May 2024
Phase: N/A
Study type: Interventional

This research will study the effect of Boswellia Sacra versus calcium hydroxide as an intracanal medicament on postoperative pain intensity measured using numerical rating scale (NRS) and bacterial load reduction reduction determined by bacterial counting using agar culture technique after root canal preparation (CFU/ml) in mandibular premolars with necrotic pulp.

NCT ID: NCT05816174 Recruiting - Clinical trials for Chronic Post Operative Pain

Longitudinal Study of Chronic Postsurgical Pain in Children and Adolescents

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

Chronic postsurgical pain is defined as pain that develops or intensifies following a surgical procedure. After major surgery, around 20% of children and adolescents develop chronic postsurgical pain, and, as part of it, negative consequences on their quality of life. Emotion-related factors such as the variability of emotions, how emotions are regulated, and how well someone is able to differentiate between different emotions have in part been studied in other types of chronic pain. To date, no study examined emotion-related factors in the development and maintenance of chronic postsurgical pain. This observational study includes five assessment time points, one before and four after major surgery, with the goal to identify emotion-related factors that increase or decrease the risk for the development of chronic postsurgical pain.

NCT ID: NCT05816109 Recruiting - Postoperative Pain Clinical Trials

The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery

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

The Effect of Superficial Cervical Plexus Block on Postoperative Recovery Quality and Pain in Anterior Cervical Spinal Surgery

NCT ID: NCT05813847 Recruiting - Hernia, Inguinal Clinical Trials

Herniorrhaphy for Postoperative Pain

Start date: April 18, 2023
Phase: Phase 3
Study type: Interventional

Subjects receive either CPL-01, positive control, or negative control after herniorrhaphy and are then followed.

NCT ID: NCT05811208 Recruiting - Pain, Postoperative Clinical Trials

Use of Pupillometry for Pain Assessment in ICU Patients With Delirium

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

Pain assessment in intensive care patients is a constant challenge. Approximately 50% to 80% of patients report pain at rest or during medical or nursing interventions (for example endotracheal suctioning, mobilization and rehabilitation, presence and care of invasive inputs, etc.). Obstacles to pain assessment and management are most often due to interference with communication due to impaired consciousness, airway support and connection to artificial pulmonary ventilation, or the effect of administered medication. Patients in intensive care are prone to delirium. Delirium can compromise patients' ability to verbalise pain for a variety of reasons (e.g. due to impaired attention, memory, thinking and language barriers). Also, pain and inadequate analgesia are risk factors for delirium. Pupillary reflex changes and their identification by automated pupillometry have yielded positive results regarding nociception assessment in adult and pediatric patients and in perioperative and postoperative care. At the same time, the response of these patients to opioid administration was investigated. The aim was to improve their analgesia. The aim of this study is to find out whether, there is an association between automated pupillometry and selected objective pain measurement scales in The Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) positive patients after surgery.

NCT ID: NCT05805423 Recruiting - Opioid Use Clinical Trials

ENDOblock: Bilateral Superficial Cervical Blocks With Local Wound Infiltration in Thyroid Surgery

Start date: April 17, 2023
Phase: N/A
Study type: Interventional

This is a single center, prospective, double-blinded randomized controlled trial comparing the efficacy of bilateral superficial cervical plexus blocks (BSCPB) with local wound infiltration vs placebo with local wound infiltration in reducing thyroid surgery postoperative pain. Primary outcomes assessed are post operative pain, quality of life/recovery, post operative nausea/vomiting and opioid use.

NCT ID: NCT05796804 Recruiting - Pain, Postoperative Clinical Trials

Erector Spinae Block Versus PENG Block for Hip Replacement

PENGESP
Start date: April 13, 2023
Phase: N/A
Study type: Interventional

THR (Total Hip Replacement) can be very painful and regional anesthesia is very effective in reducing postoperative pain. Erector Spinae Plane Block (ESPB) and PENG (pericapsular nerve group block) are alternative approaches to the hip sensitive nerve branches that resulted to be very promising for hip surgeries. However, no studies investigated the analgesic superiority of either PENG or ESPB. In our study the investigators compare PENG (with a lateral femoral cutaneous nerve block) and ESPB in terms of pain relief expressed as morphine consumption in the first 24 hours after primary THR.