Skip to main content
MedPath Trial logoMedPath TrialMedPath Trial Home
Clinical Trials/EUCTR2013-001873-25-SE
EUCTR2013-001873-25-SEActive, not recruitingPhase 1

Will intrathecal analgesia contribute to a faster recovery compared with epidural analgesia after open surgery for gynecological cancer. An open controlled randomized study. - Speed

County Council of Östergötland0 sites60 target enrollmentStarted: May 29, 2013Last updated:
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit
Drugs

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
60
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
Female

Inclusion Criteria

  • •Women 18 – 70 years.
  • •Women with gynecological cancer (suspected or verified) planned for explorative laparatomy through a middle-line with a curative purpose.
  • •WHO performance status < 2.
  • •ASA 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.
  • •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 60
  • •F.1.3 Elderly (>=65 years) yes
  • •F.1.3.1 Number of subjects for this age range 60

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 women.
  • •Women with severe psychiatric or mental disorder and any condition, which would exclude the women from conducting regional anesthesia in the standardized manner of the study.

Investigators

Sponsor
County Council of Östergötland

Similar Trials

Recruiting
Not Applicable
Comparison the effect of intrathecal analgesia with surgical ultrasound guided transverse abdominis plane block (TAP) and intrathecal analgesia for postoperative analgesia after colorectal surgeryDiseases of the digestive system
KCT0004838The Catholic University of Korea, Seoul St. Mary&#39;s Hospital64
Recruiting
Phase 3
Evaluation of adding intrathecal fentanyl and dexmedetomidine on postoperative analgesiaower limb sugary.Unspecified fracture of lower legS82.9
IRCT20110313006044N4Bandare-abbas University of Medical Sciences75
Completed
Not Applicable
Intrathecal analgesia in patients undergoing major hepatobiliary surgeryiver resectionAnalgesia following liver resectionLiver resectionSurgery - Surgical techniquesAnaesthesiology - Pain managementOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colonCancer - Liver
ACTRN12620000001998Austin Health335
Not yet recruiting
Unknown
To study the pharmacological and physical effects of adding Fentanyl as an adjuvant to hyperbaric Bupivacaine in spinal anesthesia.
CTRI/2024/02/063359Mahatma Gandhi University of medical sciences and technology
Not yet recruiting
Not Applicable
A Comparative study between 0.5% hyperbaric Bupivacaine with 20 mcg Fentanyl when taken in Single syringe and two Separate syringes for Subarachnoid block in Abdominal Hysterectomy
CTRI/2021/12/038876Mary Chacko