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TrialFinderData is for informational purposes only and does not provide medical advice. Always talk to your doctor.

Updated June 2026 · ClinicalTrials.gov

Post Graduate Institute of Medical Education and Research, Chandigarh

Reviewed by TrialFinderData Editorial Team · Updated

3 clinical trials · 3 recruiting · OTHER

Post Graduate Institute of Medical Education and Research, Chandigarh has 3 clinical trials registered on ClinicalTrials.gov, with 3 actively recruiting participants. The trials listed below cover 6 conditions across the phases listed in the sidebar. Always discuss any specific trial with your physician before contacting a study site.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About Post Graduate Institute of Medical Education and Research, Chandigarh\'s Trial Portfolio

Post Graduate Institute of Medical Education and Research, Chandigarh is a non-industry sponsor (academic medical center, hospital, foundation, or research network). Non-industry sponsors often investigate novel approaches, rare conditions, and behavioral or surgical interventions that commercial sponsors may not prioritize.

3 of Post Graduate Institute of Medical Education and Research, Chandigarh's 3 registered trials are currently recruiting — roughly 100% of the portfolio. A high recruiting share usually points to an active research pipeline with multiple programs at the enrollment stage.

Post Graduate Institute of Medical Education and Research, Chandigarh's research footprint spans Drug Resistant Epilepsy (1 trials), NAFLD (1), and Cardiac Disease (1) as the top three conditions. The full condition list, sorted by trial count, is in the sidebar.

Not Applicable is the largest single phase in Post Graduate Institute of Medical Education and Research, Chandigarh's portfolio at 33% of registered trials. The full phase breakdown appears in the sidebar.

Trials by Post Graduate Institute of Medical Education and Research, Chandigarh

RECRUITINGNCT06537986

A Neuro-cognitive and Psychosocial Intervention Module in People With Epilepsy

Patients with epilepsy, especially drug-resistant epilepsy, have a lot of cognitive \& psycho-social issues. There is little evidence pertaining to the efficacy of the various...

Sponsor: Post Graduate Institute of Medical Education and Research, ChandigarhEnrolling: 601 location
Drug Resistant Epilepsy
RECRUITINGNCT06386094

Cardiac Dysfunction in Patients with Fatty Liver Disease

Cirrhotic cardiomyopathy is seen as a blunted contractile responsiveness to stress, and/or altered diastolic relaxation with electrophysiological abnormalities, in absence of...

Sponsor: Post Graduate Institute of Medical Education and Research, ChandigarhEnrolling: 1501 location
NAFLDCardiac DiseaseFatty Liver+1
RECRUITINGPhase 4NCT06479603

RCT of Nintedanib in Fibrotic Sarcoidosis

Sarcoidosis is generally managed with outdoor immune modulatory drugs, most commonly oral steroids and at times drugs like methotrexate or azathioprine as a steroid sparing agent....

Sponsor: Post Graduate Institute of Medical Education and Research, ChandigarhEnrolling: 1201 location
Sarcoidosis, Pulmonary

How to Approach a Trial Listing

Each trial card above links to a dedicated page with the official ClinicalTrials.gov data plus a plain-English translation of the eligibility criteria. We translate technical terminology (ECOG performance status, hepatic function values, exclusionary lab thresholds) into language that a patient or caregiver can understand, but the original clinical text and the live ClinicalTrials.gov record always govern any actual eligibility decision.

Before contacting a trial site, write down questions for your treating physician using the framework on our 25 Questions guide. Discuss whether the trial fits your treatment plan, what the time commitment looks like, and whether your insurance will cover the standard-of-care portions. Trials are not a substitute for a treatment plan — they are an addition that needs medical guidance to evaluate.

Authoritative Resources

Verify any trial registration directly on ClinicalTrials.gov. For background on the FDA approval pathway that Phase 3 trials feed into, see the FDA drug approval process. For cancer-specific trial guidance, the National Cancer Institute publishes patient-oriented overviews. For global trial registrations beyond the U.S., the WHO ICTRP aggregates registries from around the world.

Frequently Asked Questions

How many clinical trials does Post Graduate Institute of Medical Education and Research, Chandigarh have on ClinicalTrials.gov?

Post Graduate Institute of Medical Education and Research, Chandigarh has 3 clinical trials registered on the federal ClinicalTrials.gov registry, of which 3 are actively recruiting participants right now. These counts come directly from the ClinicalTrials.gov API and are updated as the registry changes.

What conditions does Post Graduate Institute of Medical Education and Research, Chandigarh study?

Post Graduate Institute of Medical Education and Research, Chandigarh's registered trials cover 6 conditions on ClinicalTrials.gov, led by Drug Resistant Epilepsy (1 trial), NAFLD (1 trial), Cardiac Disease (1 trial), Fatty Liver (1 trial), MASLD - Metabolic Dysfunction-Associated Steatotic Liver Disease (1 trial). The complete condition list appears in the sidebar of this page; each condition links to a page listing every recruiting trial in that area, regardless of sponsor.

How do I join a Post Graduate Institute of Medical Education and Research, Chandigarh clinical trial?

Joining a clinical trial is a medical decision that should always involve your treating physician. Each trial page on this site includes the eligibility criteria translated into plain English alongside the official clinical text, plus the contact information that the sponsor has registered with ClinicalTrials.gov. Bring the trial information to your doctor before reaching out — they can review the full inclusion and exclusion criteria against your medical history and help you decide whether to pursue screening.

What does the trial phase mean?

Phase 1 trials test safety and dosing in small groups (often 20–80 healthy volunteers or patients). Phase 2 trials evaluate efficacy and side effects in larger groups (100–300 patients with the target condition). Phase 3 trials confirm efficacy and monitor safety in the largest groups (300–3,000+ patients) and form the basis of an FDA approval submission. Phase 4 studies happen after a treatment is approved, monitoring long-term safety and effectiveness in real-world use. Some trials register without a phase — common for device, behavioral, or observational studies.

Where does this trial data come from?

All trial data is pulled directly from the ClinicalTrials.gov API v2, the official federal trial registry maintained by the National Library of Medicine at NIH. Under FDAAA 801, most U.S. drug and device trials are required to register, making ClinicalTrials.gov the most comprehensive source. Sponsors are responsible for keeping their listings current; trial status can shift between data refreshes.

How This Sponsor Page Is Built

Every count on this page is derived directly from ClinicalTrials.gov API v2 records. Trial counts include all trials currently registered to this sponsor; the recruiting count reflects trials with status "Recruiting" or equivalent. Plain-English eligibility translations on each linked trial page preserve the original clinical text alongside an accessible version. Read the full methodology for the data pipeline and limitations.

Source: ClinicalTrials.gov API v2, maintained by the National Library of Medicine at NIH. Public domain. Cite as: "TrialFinderData. Data: ClinicalTrials.gov."

Medical disclaimer: This page is informational, not medical advice. Talk to your doctor about whether a clinical trial is right for you.

Last updated 2026-06-26 · 3 trials tracked for Post Graduate Institute of Medical Education and Research, Chandigarh.