Study to validate the questionnaire called IDSIQ™ in patients suffering from difficulties to sleep.

Phase 1

• Conditions: Insomnia disorder; MedDRA version: 20.0Level: PTClassification code 10022437Term: InsomniaSystem Organ Class: 10037175 - Psychiatric disorders; Therapeutic area: Diseases [C] - Nervous System Diseases [C10]

• Registration Number: EUCTR2016-004259-59-DE
• Lead Sponsor: Idorsia Pharmaceuticals Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-11-30
• Last Update Posted: 26 November 2018

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

- Signed informed consent prior to any study-mandated procedure;
- Male or female aged = 18 years;
- Body mass index (BMI): 18.5 = BMI (kg/m2) < 32.0;
- Insomnia disorder according to DSM-5 criteria;
- Insufficient sleep quantity evaluated according to the self-reported history and data collected in the sleep diary;
- Insomnia Severity Index score greater than or equal to 15;
- Complete the IDSIQ™ and the sleep diary questionnaire as required.
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 70
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 30

Exclusion Criteria

- Any current history of sleep disorder other than insomnia, or any lifetime history of related breathing disorder, periodic limb movement disorder, restless legs syndrome, circadian rhythm disorder, rapid eye movement behavior disorder, or narcolepsy;
- Self-reported usual daytime napping = 1 hour per day, and = 3 days per week;
- Caffeine consumption = 600 mg per day;
- Shift work within 2 weeks prior to the screening visit, or planned shift work from V1 to V3;
- Travel = 3 time zones within 1 week prior to the screening visit, or planned travel = 3 time zones from V1 to V3;
- Known severe renal impairment or know moderate or severe hepatic impairment;
- History or clinical evidence of any disease or medical condition or treatment, which may put the subject at risk of participation in the study or may interfere with the study assessments;
- Any circumstances or conditions, which, in the opinion of the investigator, may affect the subject's full participation in the study or compliance with the protocol.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified