Sigmoidal Tumour Clinical Trial
— 2013/004Official title:
RANDOMISED STUDY ABOUT POTSOTERATORY PAIN CONTROL IN LAPAROSCOPIC SIGMOIDECTOMY
The investigators would study the control of postoperative pain with peridural catheter, morphine PCA ev or Transabdominal block.
Status | Not yet recruiting |
Enrollment | 225 |
Est. completion date | April 2015 |
Est. primary completion date | April 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Age more than 18 - Laparoscopic sigmoidectomy - Informed consent firmed Exclusion Criteria: - ASA IV - Urgent surgery - Sigmoid tumour stage IV - Cronic pain treatment - No informed consent firmed - Paliative surgery |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
Spain | Corporacion Parc Tauli | Sabadell | Sabadell-Barcelona |
Spain | Corporacion Parc Tauli | Sabadell | Sabadell-barcelona |
Lead Sponsor | Collaborator |
---|---|
Corporacion Parc Tauli |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | EVA (POSTOPERATIVE PAIN) | The investigators asked the patient the postoperative pain during teh first 72 hours by EVA scale. | 72 H POSTOPERATIVE | Yes |
Secondary | ADVERSE EFFECTS | the investigators look for adverse effects | five days | Yes |