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Condition

Postoperative Complications Clinical Trials

Studies of postoperative complications, matched by condition name and medical subject headings. Start with those open to enrolment.

11,977 registered studies

In numbers

Open to volunteers
2,196
Active
2,492
With results posted
1,121
All registered
11,977

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 2,196
  • Postoperative Sore Throat

    The Effect of Compound Chamomile and Lidocaine Hydronchloride Gel as an Endotracheal Tube Lubricant on Postoperative Pharyngeal and Laryngeal Complications in Thoracic Surgery Patients

    • Not yet recruiting
    • Age: 18 to 65 years

    Total anesthesia is the most commonly used anesthesia method in clinical surgery, which can reduce hospital stay and improve patient comfort on the basis of ensuring patient surgery safety.

    Trial name
    NCT07895069
    Testing
    Polycamomile Lidocaine Gel, Lidocaine Glue
    Where
    China
    Volunteers
    330 people
    Sponsor
    The Second Affiliated Hospital of Chongqing Medical University
    Can I take part? NCT07895069
  • PND, POCD - Postoperative Cognitive Dysfunction

    Effects of Ciprofol on Perioperative Neurocognitive Function in Elderly Patients Undergoing Daytime Surgery

    • Enrolling by invitation
    • Age: 65 years and older
    • Phase 4

    As life expectancy increases, the rate of disability among elderly individuals is also rising. Elderly patients undergoing home-based rehabilitation after surgery without medical supervision may experience complications and…

    Trial name
    NCT07895407
    Testing
    Ciprofol, propofol
    Where
    China
    Volunteers
    148 people, healthy volunteers welcome
    Sponsor
    Second Affiliated Hospital of Wenzhou Medical University
    Can I take part? NCT07895407
  • Lactium, Premedication

    Lactium Premedication to Prevent Emergence Agitation

    • Not yet recruiting
    • Age: 3 to 12 years
    • Phase 3

    This biased coin sequential allocation, dose finding study will be conducted to determine the effective dose of oral lactium in 90% of children (ED90) for prevention of emergence agitation during recovery from adenotonsillectomy.

    Conditions
    Lactium, Premedication, Emergence Agitation, Adenotonsillectomy
    Trial name
    NCT07894484
    Testing
    Lactium
    Where
    Egypt
    Volunteers
    40 people
    Sponsor
    Tanta University
    Can I take part? NCT07894484
  • Pain, Postoperative

    Gabapentin to Reduce Opioid Use Postoperatively (GROUP) in Children

    • Recruiting
    • Age: Up to 17 years
    • Phase 2/3

    The primary objective of this study is to determine if the peri and post operative use of gabapentin in children reduces the need for narcotics after thoracic surgery.

    Trial name
    NCT04724252
    Testing
    Gabapentin
    Where
    United States
    Volunteers
    60 people
    Sponsor
    University of California, Davis
    Can I take part? NCT04724252
  • Anterior Cruciate Ligament Injuries, Anterior Cruciate Ligament Rupture

    Extended Post-Operative Oral Tranexamic Acid Dosing After ACL Reconstruction

    • Not yet recruiting
    • Age: 14 to 25 years
    • Phase 3

    The goal of this clinical trial is to learn whether taking oral tranexamic acid (TXA) for one week after anterior cruciate ligament (ACL) reconstruction improves recovery in adolescents and young adults aged 14 to 25 years.

    Conditions
    Anterior Cruciate Ligament Injuries, Anterior Cruciate Ligament Rupture, Pain, Postoperative
    Trial name
    NCT07880743
    Testing
    Tranexamic Acid
    Where
    6 sites in United States
    Volunteers
    100 people
    Sponsor
    Dave Bernholt
    Can I take part? NCT07880743
  • Hernia Abdominal Wall, Botox Injection

    Preoperative BOTOX® Injection for Large Ventral Hernia Repair

    • Recruiting
    • Age: 18 years and older
    • Phase 4
    • Injection or infusion
    • Surgery or procedure

    This study is for adults who need open surgery to repair a very large abdominal (ventral) hernia. This study tests whether a one-time, image-guided injection of a medicine commonly known as "BOTOX®" (onabotulinumtoxinA) into the…

    Conditions
    Hernia Abdominal Wall, Botox Injection, Hernia Incisional Ventral, Hernia Repair With Compartment Syndrome
    Trial name
    PRETOX (NCT07220382)
    Testing
    OnabotulinumtoxinA Injection, OnabotulinumtoxinA, 0.9 % Normal Saline
    Where
    United States
    Volunteers
    188 people
    Sponsor
    The Cleveland Clinic
    Can I take part? PRETOX
  • Postoperative Pain

    ESP Blocks for Posterior Spinal Fusion

    • Recruiting
    • Age: 18 to 75 years
    • Phase 4

    This prospective randomized double-blind study evaluates the efficacy of erector spinae plane (ESP) blocks on postoperative pain in patients undergoing cervical or lumbar posterior spinal fusion.

    Trial name
    NCT07228039
    Testing
    ESP Block with Bupivacaine, ESP Block with Bupivacaine + Liposomal Bupivacaine
    Where
    United States
    Volunteers
    75 people
    Sponsor
    Duke University
    Can I take part? NCT07228039
  • Knee Arthroplasty, Total, Partial Knee Arthroplasty

    Opioid Reduction and Enhanced Recovery in Orthopaedic Surgery (OREOS)-Knee

    • Not yet recruiting
    • Age: 18 years and older

    Knee replacements are the second most common surgery in Canada. Most patients recover very well but research consistently shows that 1 in 5 patients still have pain many months after surgery.

    Conditions
    Knee Arthroplasty, Total, Partial Knee Arthroplasty, Chronic Pain, Postoperative, Osteoarthritis (OA) of the Knee
    Trial name
    OREOS-K (NCT07895472)
    Testing
    Standard care, Multicomponent opioid reduction and pain management pathway
    Volunteers
    170 people
    Sponsor
    McMaster University
    Can I take part? OREOS-K
  • Wound Healing, Alveolitis of Jaw

    Effect of Curcumin Topical Spray on Wound Healing After Tooth Extraction

    • Recruiting
    • Age: 18 to 40 years

    This randomized, single-blind, controlled clinical trial aims to evaluate the effects of a topical curcumin spray on post-extraction wound healing and postoperative symptoms in adults undergoing first molar extraction.

    Conditions
    Wound Healing, Alveolitis of Jaw, Tooth Extraction, Curcumin
    Trial name
    NCT07874789
    Testing
    Curcumin Topical Spray, Chlorhexidine Topical Spray
    Where
    Turkey (Türkiye)
    Volunteers
    54 people, healthy volunteers welcome
    Sponsor
    Istanbul University
    Can I take part? NCT07874789
  • Out-of-Hospital Cardiac Arrest, Hypoxic-Ischemic Brain Injury

    Minimal Sedation Versus Standard Continuous Sedation After Out-of-Hospital Cardiac Arrest

    • Recruiting
    • Age: 18 years and older

    Most patients resuscitated from out-of-hospital cardiac arrest (OHCA) remain comatose on hospital admission and are routinely managed with continuous sedation.

    Conditions
    Out-of-Hospital Cardiac Arrest, Hypoxic-Ischemic Brain Injury, Post-Cardiac Arrest Syndrome
    Trial name
    NCT07895771
    Testing
    Minimal sedation, Standard continuous sedation
    Where
    Slovenia
    Volunteers
    100 people
    Sponsor
    University Medical Centre Ljubljana
    Can I take part? NCT07895771

Completed, with results posted

All 942
  • Hemorrhage, Surgical, Blood Loss, Surgical

    Safe and Timely Antithrombotic Removal - Ticagrelor (STAR-T)

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    Prospective, multi-center, double-blind, randomized pivotal trial to evaluate the safety and effectiveness of the DrugSorb-Antithrombotic Removal (ATR) system for intraoperative removal of ticagrelor in patients undergoing urgent…

    Conditions
    Hemorrhage, Surgical, Blood Loss, Surgical, Blood Loss, Postoperative, Hemorrhage Postoperative
    Trial name
    STAR-T (NCT04976530)
    Testing
    DrugSorb-ATR system
    Where
    29 sites in United States, Canada
    Volunteers
    140 people
    Sponsor
    CytoSorbents, Inc
    Can I take part? STAR-T
  • Pain, Pain, Postoperative

    Biofeedback Based Virtual Reality Intervention to Manage Postoperative Pain

    • Completed
    • Age: 12 to 18 years
    • Medical device
    • Results posted

    To develop and refine a technology based treatment protocol for preoperative education and training and postoperative care in children and adolescents undergoing surgery.

    Conditions
    Pain, Pain, Postoperative, Pain, Acute, Surgery
    Trial name
    NCT04943874
    Testing
    Technology Based Intervention Group 1, Technology Based Intervention Group 2
    Where
    United States
    Volunteers
    93 people
    Sponsor
    Vanessa Olbrecht
    Can I take part? NCT04943874
  • Total Knee Arthroplasty (Postoperative Pain)

    Phase 2B Study Assessing Pain Relief After Replacement of the Knee

    • Completed
    • Age: 18 to 80 years
    • Phase 2
    • Results posted

    The goal of the ATX101-TKA-004 clinical trial aims to evaluate the efficacy and safety of ATX101 1,500 mg in participants undergoing primary unilateral total knee arthroplasty.

    Trial name
    SPARK2 (NCT06799845)
    Testing
    ATX101, bupivacaine hydrochloride
    Where
    11 sites in United States
    Volunteers
    226 people
    Sponsor
    Allay Therapeutics, Inc.
    Can I take part? SPARK2
  • Pain, Postoperative, Narcotic Use

    Bupivacaine for Post-operative Pain in Mohs

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Results posted

    Mohs micrographic surgery (MMS) is regarded as the gold standard for the treatment of high-risk nonmelanoma skin cancer (NMSC). Pain after MMS peaks on the day of surgery and slowly decreases thereafter.

    Trial name
    NCT04362566
    Testing
    Bupivacaine
    Where
    United States
    Volunteers
    174 people, healthy volunteers welcome
    Sponsor
    University of Missouri-Columbia
    Can I take part? NCT04362566
  • Acute Kidney Injury

    Preop Digifab in CABG to Reduce Ouabain Levels and Prevent AKI

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Results posted

    Acute kidney injury (AKI) occurs in up to 30% of patients undergoing coronary artery bypass graft (CABG) surgery, and often requires patients to go on dialysis.

    Trial name
    NCT03810417
    Testing
    Digoxin Antibodies Fab Fragments, Baseline EO > 360 pM, EO < 360 pM
    Where
    2 sites in United States
    Volunteers
    267 people
    Sponsor
    University of Maryland, Baltimore

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