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postoperative cognitive dysfunction

Total Trials
2
Recruiting Now
2
Trial Phases
Various

ClinicalMetric tracks all active clinical trials for postoperative cognitive dysfunction sourced from ClinicalTrials.gov. Research in this area spans early-phase safety investigations through large Phase 3 confirmatory trials, conducted by NIH-funded academic centers, independent investigators, and pharmaceutical sponsors worldwide. Each listing is updated daily as new studies open enrollment and existing ones reach capacity or complete follow-up.

Trial listings include the NCT identifier, current recruitment status, phase classification, primary and secondary endpoints, estimated enrollment size, participating countries, and direct links to the full protocol on ClinicalTrials.gov. Eligibility criteria — including age range, disease stage, and prior treatment requirements — are documented for every study to help patients and clinicians assess suitability before contacting a trial site.

Frequently Asked Questions — postoperative cognitive dysfunction Clinical Trials

How many clinical trials are currently recruiting for postoperative cognitive dysfunction?
ClinicalMetric currently tracks 2 actively recruiting clinical trials for postoperative cognitive dysfunction, sourced in real time from ClinicalTrials.gov. The total number of registered studies—including those not yet enrolling or in active follow-up—is 2. Trial availability changes daily as new studies open enrollment and existing ones reach capacity.
What trial phases are available for postoperative cognitive dysfunction?
postoperative cognitive dysfunction research spans multiple clinical trial phases. Phase 1 studies evaluate safety and dosing in small groups, Phase 2 studies assess preliminary efficacy in 100–300 participants, and Phase 3 trials compare the new treatment against the standard of care in 300–3,000+ patients. Phase 4 post-approval studies monitor long-term outcomes in real-world populations.
How do I find out if I qualify for a postoperative cognitive dysfunction clinical trial?
Eligibility criteria for postoperative cognitive dysfunction trials vary by study and typically specify age range, disease stage or severity, prior treatment history, and specific diagnostic or laboratory parameters. Each listing on ClinicalMetric links to the full protocol on ClinicalTrials.gov, where inclusion and exclusion criteria are documented. Contact the sponsoring site's research coordinator directly to confirm your eligibility—your treating physician or specialist can also help identify the most appropriate trial based on your medical history and current treatment status.
Top Sponsors
Karolinska Institutet 1 trial
Columbia University 1 trial

Recruiting Clinical Trials

NCT06469515
Recruiting
Older People's Neurocognitive Recovery After Cardiac Surgery
Enrollment
220 pts
Location
Sweden
Sponsor
Karolinska Institutet
View Trial →
NCT06042699
Recruiting
Kids With Iron Deficiency and Scoliosis
Enrollment
275 pts
Location
United States
Sponsor
Columbia University
View Trial →

Related Conditions

postoperative recovery (1) cardiac surgery (1) adolescent idiopathic scoliosis (1) neuromuscular scoliosis (1) perioperative postoperative complications (1) iron deficiencies (1) anemia (1) spinal fusion (1)
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology