Postoperative Complications Clinical Trials
2 recruiting trials for Postoperative Complications. Eligibility criteria explained in plain English.
TrialFinderData lists 2 Postoperative Complications clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.
Research is led by Royal College of Surgeons, Ireland (1), Beijing Tsinghua Chang Gung Hospital (1), among the most active sponsors registered for these trials.
The most frequently studied intervention is Standard Pre-Operative Education and Physiotherapy Recommendation (other, 1 trial), followed by Pre-Operative Nurse-Led Education with Direct Physiotherapy Referral, Major Hepatobiliary Surgery.
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Recruiting Trials
Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.
Pre-Operative Nurse-Led Education With Direct Physiotherapy Referral to Reduce Post-Prostatectomy Incontinence
Urinary incontinence is a common complication following radical prostatectomy and can significantly impact quality of life. Pelvic floor physiotherapy is recommended to reduce...
Prediction Model for MINS After Major Hepatobiliary Surgery
This multi-center, prospective observational study aims to develop and validate an interpretable prediction model for Myocardial Injury After Noncardiac Surgery (MINS) in patients...
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Frequently Asked Questions
There are currently 2 clinical trials for Postoperative Complications, with 2 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.
To join a clinical trial for Postoperative Complications, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.
Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for Postoperative Complications, representing treatments closest to potential FDA approval.
Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.
Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.