Skip to main content
MedPathMedPath Home
Clinical Trials/ACTRN12610000063011
ACTRN12610000063011
Completed
Phase 4

A prospective randomized controlled trial to compare postoperative liver functions, cytokines and complications between isoflurane inhaled and propofol intravenous anesthesia in cirrhotic patients undergoing hepatectomy for hepatic carcinoma

Shanghai Rising-Star Program (No 08QA14007)0 sites60 target enrollmentJanuary 19, 2010
Share to TwitterShare to FacebookShare to LinkedInShare to Reddit

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Shanghai Rising-Star Program (No 08QA14007)
Enrollment
60
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 19, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Shanghai Rising-Star Program (No 08QA14007)

Eligibility Criteria

Inclusion Criteria

  • •1\. Elective liver resection
  • •2\. American Society of Anesthesiologists (ASA) physical status II\-III patients
  • •3\. Primary liver cancer patients who had history of hepatitis B related cirrhosis
  • •4\. undergoing combined general and epidural anesthesia

Exclusion Criteria

  • •1\.Contradictions of epidural puncture including coagulate disorder (prothrombin time (PT) longer than 15 sec or/and blood platelets count less than 10,000\)
  • •2\.Tumor size too large or small ( longitude of tumor was beyond 3\-8 cm) or estimated blood loss was large than 1000 cc.
  • •3\.Individuals in whom the regional block failed and surgery was performed under general anesthesia alone were also withdrawn from the study.
  • •4\.Indivduals fail to be performed Pringer’s maneuver due to technologic problem.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Optimal Duration of Adductor Canal Catheter Infusions for analgesia following Knee Arthroplasty
ACTRN12616000610437The Joint Studio64
Not yet recruiting
Phase 1
A study to compare the effectiveness and safety of different doses of a drug clonidine when used along with a drug bupivacaine in spinal anesthesiaHealth Condition 1: S729- Unspecified fracture of femurHealth Condition 2: S929- Unspecified fracture of foot and toeHealth Condition 3: S829- Unspecified fracture of lower leg
CTRI/2019/05/019341J J hospital
Recruiting
Phase 3
Effectiveness of Tissue plasminogen activator (TPA) for treatment of ARDS induced by Covid-19COVID-19.COVID-19 induced ARDSU07.1
IRCT20200415047080N1Tehran University of Medical Sciences30
Not yet recruiting
Not Applicable
Identifying the effectiveness of addition of an opioid drug to a combination of drugs in Ultrasonography guided adductor canal block for post operative pain relief in patients undergoing knee surgeries
CTRI/2024/03/063968SHREE KRISHNA HOSPITA
Completed
Not Applicable
A prospective randomised controlled trial to compare laparoscopic ovarian diathermy with clomiphene citrate as a first line treatment of anovulatory infertiliity in patients with polycystic ovarian syndromePolycystic ovarian syndrome (PCOS)Nutritional, Metabolic, EndocrinePolycystic ovarian syndrome
ISRCTN54264327Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)264