Sleep and Endometrial Cancer
Stopped early · Not applicable · Has a placebo group
Conditions studied: Sleep, Endometrial Neoplasms, Pain
In brief
This study proposes to test the hypothesis that zolpidem taken the night before major surgery for endometrial cancer will improve sleep efficiency and reduce post surgery pain, as well as reduce the need for analgesic medication.
Key facts
- Study ID
- NCT00936598
- Run by
- University of Pittsburgh
- People needed
- 6
- Starts
- 2009-07-01
- Expected to finish
- 2011-04-01
- Last updated by the study team
- 2014-04-24
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- be women at least 18 years old
- have clinical indications of primary endometrioid adenocarcinoma of the endometrium
- be scheduled for staging surgery by laparotomy under standardized protocols
- have the ability to communicate in English sufficient for completion of study materials
- have no neuromuscular/ movement disorders (for actigraphy purposes)
- have no uncontrolled medical, sleep, endocrine or psychiatric illness (as determined by their attending physician as part of clinical care)
- have no ongoing use of medication known to affect sleep or wake function (e.g., hypnotics, benzodiazepines, antidepressants, anxiolytics, antipsychotics, decongestants, sedating antihistamines, beta blockers, corticosteroids)
You may not qualify if…
- have a history of previous or concomitant cancer
- have an estimated life expectancy of < 6 months
- will be admitted to the hospital prior to the day of surgery
- are unable to complete study measures
- are unable to provide meaningful informed consent
Where it is running
- Magee-Womens Hospital of UPMC — Pittsburgh, Pennsylvania, United States
- UPMC Mercy — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.