Pain, Post-operative

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Review clinical trials related to Pain, Post-operative. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Does Trendelenburg Positioning During Pulmonary Recruitment Breaths Affect Post-laparoscopy Shoulder Pain

The goal of this clinical trial is to evaluate whether different positioning in the operating room during removal of laparoscopic surgical gas differs in post-surgery shoulder pain. An additional goal of this study is to evaluate whether positions change other post-surgery metrics such as bloating, time to passing gas, nausea and vomiting, and time to oral intake. Researchers will compare Trendelenburg positioning where your head is tilted down to supine (level or flat) positioning during removal of surgical gas. Participants will be asked to complete brief surveys at 24 and 72-hours post-surgery.

Participants needed: 120
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Ankita GuptaUpdated: Jun 8, 2026
Eligibility criteria

Robot-assisted laparoscopic surgery for benign gynecologic indication [+2]

Patients with baseline opioid use [+5]

Status: Recruiting

Comparing Analgesic Regimen Effectiveness and Safety for Surgery for Kids Trial

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. Eligible participants will be randomized to prescription of 1 of 2 groups of medications (Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) plus acetaminophen or low dose opioids with the NSAIDs plus acetaminophen. The key question the study seeks to answer is which option will have the best outcomes and with the fewest side effects?

Participants needed: 900
Trial details
Phase: Phase 4Age: 12-20Biological sex: AllType: InterventionalSponsor: University of MichiganUpdated: Mar 4, 2026Locations: 4
Eligibility criteria

No significant analgesic medication use before surgery as defined in the protoco... [+1]

Anticipated other surgery within 12 months [+6]

Status: Recruiting

A Study to Reduce Persistent Post-mastectomy Pain Using Opioid-free Anesthesia

In 230 patients undergoing mastectomy, the investigators will compare opioid-free anesthesia (OFA) versus conventional opioid-based anesthesia in terms of chronic pain. The enrolled patients will be randomly assigned into two groups with 1:1 ratio. Chronic pain will be evaluated at 1 year after mastectomy based on the Breast Cancer Pain Questionnaire (BCPQ). Baseline pain sensitivity test and psychologic evaluation will be done before operation.

Participants needed: 230
Trial details
Age: 19-80Biological sex: FemaleType: InterventionalSponsor: Gangnam Severance HospitalUpdated: Nov 21, 2025Locations: 1
Eligibility criteria

All of patients will undergo mastectomy with or without immediate breast reconst...

Previous history of breast surgery [+9]

Status: Recruiting

Preemptive Ibuprofen Effects on Pain Perception Following Extraction and Bone Graft

The goal of this randomized clinical trial is to compare patient-reported pain and oral health-related quality of life during the first postoperative week following extraction and bone graft surgery in patients who received preemptive ibuprofen versus placebo. Participants will receive ibuprofen 600mg or placebo by mouth with water 1 hour prior to extraction and bone graft surgery. The primary question it aims to answer is: • Does preemptive ibuprofen have an effect on postoperative pain 1 hour following extraction and bone graft surgery compared to placebo? Secondary questions are: * Does preemptive ibuprofen have an effect on pain during the first 3 postoperative hours and 7 postoperative days following extraction and bone graft surgery compared to placebo? * Does preemptive ibuprofen have an effect on oral health-related quality of life during the 7 postoperative days following extraction and bone graft surgery compared to placebo?

Participants needed: 50
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Marquette UniversityUpdated: Sep 27, 2024Locations: 1
Eligibility criteria

Age >18 years [+3]

Pregnancy [+14]