# Decision Support for Parents Receiving Information About Child's Rare Disease

> **NCT01875640** · — · COMPLETED · sponsor: **University of Michigan** · enrollment: 63 (actual)

## Conditions studied

- Disorder of Sex Development
- Intersex Conditions
- Congenital Adrenal Hyperplasia
- Hypospadias

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT01875640
- **Lead sponsor:** University of Michigan
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** COMPLETED
- **Start date:** 2013-06
- **Primary completion:** 2016-05
- **Final completion:** 2017-12
- **Target enrollment:** 63 (ACTUAL)
- **Last updated:** 2024-05-08

## Collaborators

- [object Object]
- [object Object]
- [object Object]
- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01875640

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01875640, "Decision Support for Parents Receiving Information About Child's Rare Disease". Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/clinical/NCT01875640. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*