Rare hand deformity study seeks answers from medical records

NCT ID NCT07404514

Not yet recruiting Knowledge-focused Sponsor: Hopitaux de Saint-Maurice Source: ClinicalTrials.gov ↗

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at medical records and parent questionnaires from about 28 children with a rare hand condition called longitudinal ulnar deficiency. The goal is to better understand how the condition changes over time and what factors lead to surgery. No new treatments or tests are being given; the study only reviews existing information.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to: If successful, this study could lead to better guidelines for when surgery is helpful for children with this rare hand condition.
What could go wrong: This is a small, observational study that only looks at past data and parent reports. It will not test any new treatment, so it cannot directly improve care.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for OCCUPATIONAL THERAPY are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

ulnar hemimelia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

OCCUPATIONAL THERAPY ULNAR HAND DEFORMITY ULNAR LONGITUDINAL DEFICIENCY ULNAR LONGITUDINAL DEFICIT

Contacts and locations

Locations

Hôpitaux Paris Est Val-de-Marne - Centre de Référence des Malformations des Membres

Saint-Maurice, 94410, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.