# Oxalate Excretion Profile in Patients With a Heterozygous Mutation of the AGXT (Alanine-glyoxylate Aminotransferase) Gene

> **NCT06283082** · NA · COMPLETED · sponsor: **Hospices Civils de Lyon** · enrollment: 25 (actual)

## Conditions studied

- Hyperoxaluria (Disorder)

## Interventions

- **DIAGNOSTIC_TEST:** Lithiasis assessment

## Key facts

- **NCT ID:** NCT06283082
- **Lead sponsor:** Hospices Civils de Lyon
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2024-12-11
- **Primary completion:** 2025-11-08
- **Final completion:** 2025-12-01
- **Target enrollment:** 25 (ACTUAL)
- **Last updated:** 2026-05-06


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06283082

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06283082, "Oxalate Excretion Profile in Patients With a Heterozygous Mutation of the AGXT (Alanine-glyoxylate Aminotransferase) Gene". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06283082. Licensed CC0.

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