Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Outcome Measure:

EVA (POSTOPERATIVE PAIN)

Outcome Description:

The investigators asked the patient the postoperative pain during teh first 72 hours by EVA scale.

Outcome Time Frame:

72 H POSTOPERATIVE

Safety Issue:

Yes

Principal Investigator

PUJOL GEMMA, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Corporacion Parc Tauli

Authority:

United States: Food and Drug Administration

Study ID:

CIR TAP 2013

NCT ID:

NCT01825993

Start Date:

April 2013

Completion Date:

April 2015

Related Keywords:

• Sigmoidal Tumour
• Peridural catheter
• Morphine PCA
• Transabdominal Block
• laparoscopic sigmoidectomy