Cure My Disease

Don't miss your cure!

Log in / Sign up

Achalasia, familial esophageal

MONDO:0100457

An instance of achalsia that is caused by an inherited genomic modification in an individual.

Also known as: achalasia, familial esophageal

6 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Hereditary disease (176) Digestive system disorder (160) Achalasia (33) Esophageal disorder (20) Human disease (14) Upper digestive tract disorder (6) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)

Trials to join now! 4 Not yet recruiting 1 Completed 1

New hope for preventing Post-Surgery confusion in seniors

Symptom relief Completed

This study tested whether giving a small amount of s-ketamine during chest surgery could reduce the risk of postoperative delirium (sudden confusion) in patients aged 60 and older. Over 500 participants were randomly assigned to receive either s-ketamine or another drug (dexmedet…

Phase: EARLY_PHASE1 • Sponsor: Affiliated Cancer Hospital & Institute of Guangzhou Medical University • Aim: Symptom relief

Last updated Jun 27, 2026 12:28 UTC