Skip to content

AMIloride for the treatment of Nephrogenic Diabetes insipidus for patients with bipolar disorder treated with lithium: a randomized controlled trial - AMIND

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2021-003600-41-FR
Enrollment
10
Registered
2021-09-21
Start date
2022-01-25
Completion date
Unknown
Last updated
2024-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Trade Name: MODAMIDE 5 mg Product Name: AMILORIDE Pharmaceutical Form: Tablet INN or Proposed INN: AMILORIDE CAS Number: 2609-46-3 Concentration unit: mg milligram(s) Concentration type: equal Concent

Sponsors

Assistance Publique – Hôpitaux de Paris (AP-HP)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: NA Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 9 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 1

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Main Objective: NA;Secondary Objective: NA;Primary end point(s): NA;Timepoint(s) of evaluation of this end point: NA

Secondary

MeasureTime frame
Secondary end point(s): NA;Timepoint(s) of evaluation of this end point: NA

Countries

France

Contacts

Public ContactSEYMOUR-INAMO

APHP

karine.seymour@aphp.fr+3301 44 84 17 42

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026