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OpenTrials
Completed

NCT Number: NCT01211743

Oxidative Stress in Standard Laparoscopic vs Single Port Cholecystectomy

Study of Oxidative Stress Markers in order to assess whether there are differences between standard laparoscopic cholecystectomy vs single port cholecystectomy for uncomplicated cholelithiasis

Completed

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Key information

Age range

30 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

G Hatzikosta General Hospital of Ioannina

Ioannina, Epirus, 45001, Greece

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Uncomplicated cholelithiasis American Society of Anesthesiologists (ASA) I or II No previous operations in upper abdomen Body mass index (BMI) -

Exclusion criteria

Cholecystitis ASA > II BMI>30 Previous operations in upper abdomen Previous operations in intestine Smokers Alcohol Drugs

-

Treatment and study plan

Laparoscopic cholecystectomy

Other

Standard 4 port laparoscopic cholecystectomy

Single incision laparoscopic cholecystectomy

Other

One port placed through the umbilicus

Sponsors and collaborators

Lead sponsor

G. Hatzikosta General Hospital

Other

Collaborators

  • Demokrition University of Thrace
  • University of Ioannina

Registry information

Official study title

Study of Oxidative Stress in Standard Laparoscopic vs Single Port Cholecystectomy for Uncomplicated Cholelithiasis (Lap vs SILS)

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Sep 29, 2010
Registry last updated
Sep 29, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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