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Laparoscopic Gas Pressure and Postoperative Pain Score

Does Laparoscopic Entrance and Intraoperative Intraabdominal Gas Pressure Effect Postoperative Pain Score

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03623399
Enrollment
195
Registered
2018-08-09
Start date
2018-08-07
Completion date
2019-05-31
Last updated
2018-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Laparoscopy, Postoperative Pain

Keywords

postoperative pain, Intraabdominal laparoscopic gas pressure

Brief summary

Aim of the study is to determine the effect of different laparoscopic intraoperative intraabdominal gas (CO2) pressures on the extent of postoperative pain scores.

Detailed description

In this study investigator planned to randomize patients into three groups ; in the first group abdominal entrance pressure will be 15 mmhg and intraoperative pressure will be 15 mmhg too ; in the second group again entrance pressure will be 15 mmhg , intraoperative pressure will be 12 mmhg ; and in the thirth group both entrance and intraoperative pressures will be 12 mmhg. During operation intraoperative mean pressures will be recorded every 15 minutes , also end tidal CO2 pressures will also assesed by the anesthesiologist. Every participant will take , same standard analgesics ; 2 mg/kg contramal and 1 gr i.v. paracetamol at the end of the operation ; except the ones who has allergy to these analgesics. At postoperative 6 th and 24 th hours patients will be asked to execute the visual analogue score (VAS) form to assess the pain . Only patients with benign gynecologic pathologies will be included in to the study and informed consent forms will be taken from all participants.

Interventions

PROCEDURElow gas pressure laparoscopy

To apply different CO2 entrance and intraoperative pressures

Sponsors

Seda Yuksel Simsek
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* benign gynecologic pathologies which requires laparoscopic surgery

Exclusion criteria

* patients who has malign gynecologic pathologies

Design outcomes

Primary

MeasureTime frameDescription
postoperative pain scoresPostoperative 6 th hourDifference between pain scores of participitants according to differing gas pressures applied.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSeda YUKSEL SIMSEK, M.D.
dryukselseda@hotmail.com+905359112244
Backup ContactErhan SIMSEK, Ass. Prof.
drsimsekerhan@hotmail.com+905334146299

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026