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Individualized Pneumoperitoneum Pressure in Colorectal Laparoscopic Surgery (IPPCollapseI)

L

La Fe University and Polytechnic Hospital

Status

Completed

Conditions

Individualized Pneumoperitoneum Pressure

Treatments

Procedure: Laparoscopic colorectal surgery

Study type

Observational

Funder types

Other

Identifiers

NCT03000465
2015/0094

Details and patient eligibility

About

Optimizing all factors that increase the intra-abdominal volume and performing an individualized strategy should allow us to reduce the pneumoperitoneum insufflation pressure while maintaining optimal surgery conditions for a laparoscopic colorectal surgery, compared to the standard strategy of maintaining fixed intra-abdominal insufflation pressures (12-15 mmHg).

Full description

In the context of multimodal rehabilitation in colorectal laparoscopic surgery (Fast Track or ERAS (Enhance Recovery After Surgery)) multiple strategies have been introduced that have managed to improve patient recovery, decrease postoperative complications, decrease hospital days and decrease the overall costs per process.

The possibility of performing individualized colorectal laparoscopic surgery with the minimum insufflation pressure guaranteeing optimal surgical conditions has not been evaluated and this would allow us to reduce the impact of surgery on the patient, decrease perioperative morbidity and improve patient recovery.

In our study, abdominal compliance, Pv0 and maximal Pv were determined during the initial performance of the pneumoperitoneum, and then a stepwise protocol for the reduction of intra-abdominal pressure (IAP) insufflation was stablished with evaluation by the surgeons, until reaching the minimal insufflation IAP in which optimal surgical conditions are maintained.

Enrollment

92 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Over 18 years of age
  • ASA I-III (American Society of Anesthesiologists physical status classification)
  • Signed informed consent
  • Absence of cognitive deficit

Exclusion criteria

  • Urgent surgery
  • Pregnancy or breastfeeding
  • Immune Disorder
  • Advanced renal, hepatic or cardiopulmonary disease
  • Negative to participate in the study
  • Under 18 years
  • Inability to give consent
  • Associated neuromuscular disorders
  • Allergy to rocuronium/sugammadex
  • Contraindication for use of rocuronium/sugammadex

Trial design

92 participants in 1 patient group

Patients
Description:
Patients undergoing laparoscopic colorectal surgery
Treatment:
Procedure: Laparoscopic colorectal surgery

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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