A Non-inferiority Study With Two Treatment Arms Eszopiclone 3 mg Versus Zopiclone 7.5 mg - for the Treatment of Insomnia

INSOMNIA Clinical Trial

— Eszo  

Official title:

A Phase III, Non-inferiority, Double-blind, Unicenter Clinical Trial With Two Treatment Arms - Test Group With Eszopiclone 3 mg Versus Zopiclone 7.5 mg - for the Treatment of Insomnia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01100164
• Other study ID #: EF097
• Status: Completed
• Phase: Phase 3
• First received: April 5, 2010
• Last updated: July 24, 2015
• Start date: March 2011
• Est. completion date: April 2012

Study information

• Verified date: March 2010
• Source: Eurofarma Laboratorios S.A.
• Contact: n/a
• Is FDA regulated: No
• Health authority: Brazil: Ethics CommitteeBrazil: National Health Surveillance Agency
• Study type: Interventional

Clinical Trial Summary

The primary objective of the study is to determine whether eszopiclone (Eurofarma) is non-inferior to the reference drug zopiclone (Imovane®, Sanofi-Aventis) in the treatment of insomnia.

Description:

The primary objective of the study is to determine whether eszopiclone (Eurofarma) is non-inferior to the reference drug zopiclone (Imovane®, Sanofi-Aventis) in the treatment of insomnia. To that end, the latency to persistent sleep (LPS) will be used as a primary endpoint at the end of the treatment, measured by polysomnography.

The secondary objectives and endpoints of this study are as follows:

• To evaluate the efficiency of eszopiclone compared to zopiclone by means of the patient's clinical history, using as secondary endpoints:

• Variables of the sleep diary of the Associação Fundo de Incentivo à Psicofarmacologia (see Appendix A), namely:

• Latency time to the beginning of the sleep;

• Frequency of night wake-ups;

• Time awake during bedtime;

• Early morning awakening;

• Total time in bed;

• Sleep efficiency;

• Sleep variables measured by actigraph;

• Insomnia Severity Index (see Appendix B);45

• Pittsburgh Sleep Quality Index (see Appendix C);46

• To evaluate the safety of eszopiclone compared to zopiclone by means of adverse events in each study arm.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 263
• Est. completion date: April 2012
• Est. primary completion date: March 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 64 Years

Eligibility

Inclusion Criteria:

• Sign the informed consent form for the study;

• Be = 20 to = 64 years old;

• Have diagnosis of symptomatic primary insomnia for at least 3 months;

• Have polysomnography conducted at least 90 days before the inclusion in the study with sleep time less than 6.5 hours and sleep latency = 20 minutes;

• Be able not to take any insomnia medication for 14 days before randomization to the study (washout period).

Exclusion Criteria:

• Diagnosis of other sleep disorder by polysomnography conducted 90 days before the inclusion in the study;

• Use of any medication affecting the sleep, such as psychotropic, hypnotic or antihistamine agents for at least 15 days before the inclusion in the study;

• Use of any herbal supplement for insomnia or melatonin during the 14 days before entering the study;

• Current use of liver metabolized medication, especially those metabolized through the cytochrome P450 enzyme complex, especially through the CYP3A4 and/or CYP2E1 routes;

• History of daily use of alcohol beverages in quantities equivalent - from the ethanol standpoint - to two cans of beer a day (35 g of alcohol/day);

• History of substance abuse or dependence;

• Patients with severe co-morbidities (at the investigator's opinion);

• Presence of liver disorders, cirrhosis or liver failure;

• Presence of psychiatric disorders diagnosed at the adult life or currently under treatment;

• Pregnant and breastfeeding women and women who want to become pregnant during the study period and who refuse to use a proper contraceptive methods during the study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• INSOMNIA

Intervention

Drug:
• Eszopiclone
Eszopiclone - once a day (30 minutes before lying down to sleep for a period of 4 weeks of treatment)
• Zopiclone
Zopiclone - once a day (30 minutes before lying down to sleep for a period of 4 weeks of treatment)

Locations

Country	Name	City	State
Brazil	CRDB - Clinical Research & Development Brazil	São Paulo

Sponsors (1)

Lead Sponsor	Collaborator
Eurofarma Laboratorios S.A.

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Latency to persistent sleep measured by polysomnography	Determine whether eszopiclone is noninferior to the reference drug zopiclone (Imovane®) in the treatment of insomnia. The latency to persistent sleep will be used as a primary endpoint at the end of the treatment, measured by polysomnography	4 weeks	Yes
Secondary	Efficiency using the variables latency time to persistent sleep, frequency of night awakenings, time awake during bedtime, early morning awakening, total time in bed, total time awake and sleep efficiency		6 weeks	Yes