AzTrials
AzTrials

Drug or intervention

Ibuprofen Clinical Trials

Studies that test Ibuprofen, alone, with other treatments or as the comparison.

1,119 registered studies

In numbers

Open to volunteers
127
Active
145
With results posted
246
All registered
1,119

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

Open to volunteers

All 127
  • Fibroadenoma, Breast Fibroadenoma

    Management of Breast Fibroadenoma: Comparing Observation, Microwave Ablation, and Surgical Excision

    • Not yet recruiting
    • Age: 18 to 40 years
    • Surgery or procedure

    The purpose of this study is to evaluate and compare three different management strategies for benign breast fibroadenoma: conservative management with clinical and radiological follow-up (observation), ultrasound-guided…

    Conditions
    Fibroadenoma, Breast Fibroadenoma, Benign Breast Disease
    Trial name
    NCT07890766
    Testing
    Ultrasound-guided percutaneous microwave ablation, Conventional open surgical excision
    Where
    Egypt
    Volunteers
    60 people
    Sponsor
    Sohag University
    Can I take part? NCT07890766
  • Surgery, Pain, Post Operative

    Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial

    • Recruiting
    • Age: 12 to 20 years
    • Phase 4

    This trial is being completed to compare two commonly used options to treat pain after discharge from surgery. Participants that undergo tonsil removal, gallbladder removal, and knee scope will be eligible to enroll.

    Trial name
    CARES for Kids (NCT06671002)
    Testing
    NSAID, Opioid, Acetaminophen
    Where
    9 sites in United States
    Volunteers
    900 people
    Sponsor
    University of Michigan
  • Musculoskeletal Pain

    Musculoskeletal Outcomes Using Tylenol/Ibuprofen vs. Oral Steroids in New Injuries

    • Enrolling by invitation
    • Age: 18 years and older
    • Phase 4
    • Pill or oral medicine

    In this pilot study, the investigators aim to compare two short-term pain relief methods administered over the course of 6 days in the setting of acute musculoskeletal (MSK) pain: 1.

    Trial name
    MOTION (NCT07393503)
    Testing
    Methylprednisolone 4Mg Tab, Acetaminophen 500Mg Tab, Ibuprofen 200Mg Oral Tablet
    Where
    United States
    Volunteers
    60 people
    Sponsor
    State University of New York at Buffalo
    Can I take part? MOTION
  • Appendectomy, Laparoscopic, Acute Appendicitis

    Feasibility and Safety of a Pediatric ERAS Protocol for Laparoscopic Appendectomy

    • Recruiting
    • Age: 5 to 18 years

    Acute appendicitis is the most common surgical emergency in children. Despite the widespread adoption of laparoscopic appendectomy, postoperative care still varies widely between institutions, with prolonged fasting, opioid-based…

    Conditions
    Appendectomy, Laparoscopic, Acute Appendicitis, Pediatric Surgery, ERAS
    Trial name
    NCT07643285
    Testing
    Comprehensive 20-Item Pediatric ERAS Protocol
    Where
    Turkey (Türkiye)
    Volunteers
    100 people
    Sponsor
    Ahmet Burak Doğan, MD
    Can I take part? NCT07643285
  • Pain, Postoperative Pain

    Comparison of the Effectiveness of Midpoint Transverse Process to Pleura (MTP) Block and Erector Spinae Plane (ESP) Block in Video-Assisted Thoracoscopic Surgery (VATS) at RS Ngoerah

    • Recruiting
    • Age: 18 to 65 years
    • Surgery or procedure

    This randomized, double-blind controlled trial compares two ultrasound-guided fascial plane blocks, the midpoint transverse process to pleura (MTP) block and the erector spinae plane (ESP) block, for postoperative analgesia in…

    Trial name
    MESA-VATS (NCT07868484)
    Testing
    Midpoint Transverse Process to Pleura (MTP) block, Erector spinae plane (ESP) block
    Where
    Indonesia
    Volunteers
    51 people
    Sponsor
    Udayana University
    Can I take part? MESA-VATS
  • Postsurgical Pain Management, Postsurgical Pain, Chronic

    An Artificial Intelligence Driven Approach to Optimize Patient Selection for a Transitional Pain Service

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 3
    • Medical device
    • Surgery or procedure

    The goal of this clinical trial is to learn whether a pain-management program called a Transitional Pain Service can help prevent long-term pain and reduce opioid needs after surgery in adult surgical patients who may be at…

    Conditions
    Postsurgical Pain Management, Postsurgical Pain, Chronic, Opioid Use After Surgery
    Trial name
    TPS-Select (NCT07296770)
    Testing
    TPS-Select, Pharmacologic Pain Management, Interventional Pain Procedures
    Where
    United States
    Volunteers
    474 people
    Sponsor
    University of California, San Francisco
    Can I take part? TPS-Select
  • Electronic Moxibustion, Low Back Pain

    Study on the Effect of Electronic Moxibustion on Non-Specific Low Back Pain in Young Adults

    • Not yet recruiting
    • Age: 18 to 40 years

    This is an interventional clinical study. A total of 90 subjects aged 18 to 40 years are planned to be recruited. The subjects have low back pain that affects daily work and life, resulting in reduced exercise tolerance or…

    Conditions
    Electronic Moxibustion, Low Back Pain, Muscle Hardness
    Trial name
    NCT07858188
    Testing
    Electronic Moxibustion, ibuprofen or celecoxib analgesics
    Where
    China
    Volunteers
    90 people
    Sponsor
    Nanfang Hospital, Southern Medical University
  • Pelvic Organ Prolapse (POP), Postoperative Pain

    Suzetrigine Following Urogynecologic Surgery: Investigation of Postoperative Pain Management

    • Not yet recruiting
    • Age: 40 to 80 years
    • Phase 4

    The goal of this clinical trial is to determine whether suzetrigine, when added to standardized multimodal postoperative analgesia improves pain control and reduces opioid consumption after apical suspension surgery for pelvic…

    Conditions
    Pelvic Organ Prolapse (POP), Postoperative Pain, Urogynecology
    Trial name
    SUSI (NCT07856654)
    Testing
    Suzetrigine
    Where
    United States
    Volunteers
    48 people, healthy volunteers welcome
    Sponsor
    Aditi Talkad
    Can I take part? SUSI
  • Nail Diseases

    Post-op Analgesia of Nail Unit Procedures

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 4

    The purpose of this study is to directly compare the efficacy of suzetrigine vs. oxycodone+acetaminophen vs. alternating acetaminophen/ibuprofen in controlling post-operative pain after the following nail unit procedures.

    Trial name
    NCT07820969
    Testing
    Suzetrigine, Oxycodone/Acetaminophen, Acetaminophen
    Where
    United States
    Volunteers
    45 people
    Sponsor
    University of Miami
  • Pain, Postoperative, Rebound Pain

    Intravenous Dexamethasone With Single-Shot Versus Continuous Brachial Plexus Block for Rebound Pain After Shoulder Surgery

    • Recruiting
    • Age: 19 to 79 years
    • Phase 4
    • Injection or infusion
    • Surgery or procedure

    Shoulder surgery often causes severe pain after the operation. To control this pain, doctors commonly perform a nerve block (interscalene brachial plexus block), which numbs the shoulder area.

    Conditions
    Pain, Postoperative, Rebound Pain, Shoulder Injuries, Rotator Cuff Injuries
    Trial name
    NCT07699744
    Testing
    Dexamethasone (IV), Single-shot interscalene brachial plexus block, Continuous interscalene brachial plexus block
    Where
    South Korea
    Volunteers
    92 people
    Sponsor
    Seoul National University Hospital
    Can I take part? NCT07699744

Completed, with results posted

All 202
  • Opioid Use

    Opioid Analgesic Reduction Study

    • Completed
    • Age: 18 years and older
    • Phase 3
    • Results posted

    The goal is to provide health care professionals, including dentists, with the best possible evidence for clinical decision making when deciding upon analgesics for acute post-surgical pain management, a double-blind, stratified…

    Trial name
    OARS (NCT04452344)
    Testing
    opioid-containing analgesic, two over-the-counter analgesics
    Where
    5 sites in United States
    Volunteers
    1,815 people, healthy volunteers welcome
    Sponsor
    Rutgers, The State University of New Jersey
    Can I take part? OARS
  • Pain Measurement

    Comparison Between Dexamethasone and Ibuprofen on Pain Prevention and Control Following Surgical Implant Placement

    • Completed
    • Age: 18 to 65 years
    • Phase 4
    • Results posted

    Background and aim: Postoperative pain is an adverse effect of oral surgeries and may therefore be prevented or minimized. This study compares the efficacy of preemptive ibuprofen and dexamethasone protocols in pain prevention…

    Trial name
    CBDIPPCFSIP (NCT02763059)
    Testing
    Ibuprofen 600 mg, Dexamethasone 4 mg, Acetaminophen 1000 mg
    Volunteers
    132 people, healthy volunteers welcome
    Sponsor
    King Abdulaziz University
    Can I take part? CBDIPPCFSIP
  • Pain, Postoperative Pain

    Efficacy of Different Drugs to Control Post Root Canal Treatment Pain

    • Completed
    • Age: 18 to 60 years
    • Phase 2
    • Results posted

    Root canal therapy will ideally eliminate post-endodontic pain but occasionally analgesics are needed to diminish the pain [Owatz et al 2007].

    Conditions
    Pain, Postoperative Pain, Irreversible Pulpitis
    Trial name
    NSAID (NCT02417337)
    Testing
    Paracetamol, Ibuprofen, Mefenamic Acid
    Where
    Sudan
    Volunteers
    185 people, healthy volunteers welcome
    Sponsor
    University of Khartoum
    Can I take part? NSAID
  • Low Back Pain

    Acute Low Back Pain. Topical Diclofenac and Oral Ibuprofen.

    • Completed
    • Age: 18 to 69 years
    • Phase 4
    • Results posted

    This is a randomized, double-blind placebo-controlled study comparing two different treatments for acute low back pain: oral ibuprofen and topical diclofenac.

    Trial name
    NCT04611529
    Testing
    Ibuprofen 400 mg, Topical diclofenac
    Where
    United States
    Volunteers
    198 people
    Sponsor
    Montefiore Medical Center
    Can I take part? NCT04611529
  • Analgesia

    Study of Post-Herniorrhaphy Non-opioid MMA Regimens

    • Completed
    • Age: 18 years and older
    • Phase 3
    • Medical device
    • Results posted

    This is a Phase 3b, open-label study to assess postoperative opioid use in subjects undergoing unilateral open inguinal herniorrhaphy with intraoperative administration of HTX-011 and a postoperative non-opioid multimodal…

    Trial name
    NCT03907176
    Testing
    HTX-011, Luer lock applicator, Ibuprofen
    Where
    30 sites in United States
    Volunteers
    209 people
    Sponsor
    Heron Therapeutics

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