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A Prospective Open-Label Extension Study of Gaboxadol in Primary Insomnia

Primary Purpose

Primary Insomnia

Status
Completed
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Gaboxadol
Sponsored by
H. Lundbeck A/S
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Insomnia focused on measuring Primary insomnia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: patients with a diagnosis of primary insomnia

Sites / Locations

  • Non-US study, principal location:

Outcomes

Primary Outcome Measures

Safety
Tolerability

Secondary Outcome Measures

Full Information

First Posted
September 13, 2005
Last Updated
March 29, 2007
Sponsor
H. Lundbeck A/S
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1. Study Identification

Unique Protocol Identification Number
NCT00209950
Brief Title
A Prospective Open-Label Extension Study of Gaboxadol in Primary Insomnia
Official Title
A Prospective Open-Label Extension Study (to Study 99784) of Gaboxadol in Primary Insomnia
Study Type
Interventional

2. Study Status

Record Verification Date
March 2007
Overall Recruitment Status
Completed
Study Start Date
July 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
H. Lundbeck A/S

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To evaluate the safety and tolerability of gaboxadol in primary insomnia
Detailed Description
To evaluate long-term safety of gaboxadol in healthy adults.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Insomnia
Keywords
Primary insomnia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Gaboxadol
Primary Outcome Measure Information:
Title
Safety
Title
Tolerability

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with a diagnosis of primary insomnia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Please contact: Annelies van der Hammen Legters
Organizational Affiliation
H. Lundbeck A/S
Official's Role
Study Director
Facility Information:
Facility Name
Non-US study, principal location:
City
Regensburg
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

A Prospective Open-Label Extension Study of Gaboxadol in Primary Insomnia

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