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Recovery and Analgesia After Surgery for Gynecological Cancer | Clinical Trials | Clareo Health

COMPLETEDPHASE4

Recovery and Analgesia After Surgery for Gynecological Cancer

Will Intrathecal Analgesia Contribute to a Faster Recovery Compared With Epidural Analgesia After Open Surgery for Gynecological Cancer. An Open Controlled Randomized Study.

NCT02026687•Lena Nilsson

View on ClinicalTrials.gov

Summary

The purpose of the study is to compare epidural analgesia and intrathecal analgesia for explorative laparotomy through a middle-line incision for gynecological cancer in a fast track program to se if there is any difference in recovery. Length of stay is analyzed together with self-rate quality of life.

Eligibility

Age

18 - 70 years

Sex

FEMALE

Healthy Volunteers

Inclusion Criteria

•Women with gynecological cancer (suspected or verified) planned for explorative laparotomy through a middle-line incision with a curative purpose.
•WHO performance status \< 2.
•American Society of Anesthesiologists class 1-2.
•Women that understand and can express themselves in Swedish.
•Women that after verbal and written information accept participation in the study and have signed an informed consent.

Exclusion Criteria

•Women where surgery is expected to include part/s, other than the abdominal surgery, where intrathecal or epidural analgesia is not expected to be effective
•Women with contra indications for intrathecal or epidural anesthesia.
•Women who are physically disabled and therefore nor expected to be mobilized on the day after surgery in the same way as non-disabled.
•Women with a mental retardation that makes it impossible to fill in the relevant questionnaires or makes it impossible to understand the meaning of participation, or if it is ethically doubtful to include the woman.
•Women with psychiatric or mental disorder that according to the responsible physician makes it unsuitable to participate in the study .

Locations (1)

University Hospital

Linköping, Sweden

Key Dates

Start Date

March 1, 2014

Primary Completion Date

April 1, 2016

Completion Date

May 1, 2016

Last Updated

September 24, 2019

Enrollment

ACTUAL participants

Conditions

Gynecological Cancer

Interventions

Epidural

DRUG

Intrathecal

DRUG

Gene and Molecular Pathways of Ozone Treatment Response in Gynecological Tumor Patients With Chronic Pelvic Pain Secondary to Cancer Treatment

NCT06816095

Chronic Pelvic Pain Syndrome (CPPS)Radiation-Induced Disorder+3 more

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RECRUITINGNA

Laparoscopic Surgical Systems for Gynecological and Remote Surgical Treatment.

NCT06676267

Gynecological Cancer

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 24, 2019Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Recovery and Analgesia After Surgery for Gynecological Cancer

Inclusion Criteria

Exclusion Criteria

Gene and Molecular Pathways of Ozone Treatment Response in Gynecological Tumor Patients With Chronic Pelvic Pain Secondary to Cancer Treatment

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