An interventional study of Bupivacaine in Postoperative Complications, sponsored by Wolfson Medical Center. Status unknown at 1 site in Israel. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-05-09.
Sponsored by Wolfson Medical Center · Not applicable, Interventional, and Supportive care
A comparison between local and intraperitoneal analgetics to placebo, during laparoscopy, regarding post operative pain.
4 randomly assigned groups. Grop 1 will get sub cutaneous and intraperitoneal marcain. Grop 2 will get sub cutaneous marcaine and intraperitoneal saline. Grop 3 will get sub cutaneus saline and intraperitoneal marcaine. Grop 4 will get ub cutaneous and intraperitoneal saline
5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.
This study's planned enrollment of 120 is above the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.
Browse Pain, Postoperative studies →Wolfson Medical Center is the lead sponsor of 113 studies on the registry; 16 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Sub cutaneous Bupivacaine+ Intraperitoneal bupivacaine
Drug: Bupivacaine
Sub cutaneous Bupivacaine+ Intraperitoneal Nacl 0.9%
Drug: Bupivacaine
Sub cutaneous Nacl 0.9%+ Intraperitoneal bupivacaine
Drug: Bupivacaine
Sub cutaneous Nacl 0.9%+ Intraperitoneal Nacl 0.9%
Drug: Bupivacaine
Sub cutaneous and/or Intraperitoneal Marcaine application
Also known as: Marcaine
Pain level during movement, 8 hours after laparoscopy
Time frame: 8 hours
Plan to share: No
This study is status unknown, as verified in May 2018. You cannot join it, but the record below documents what was studied.
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Wolfson Medical Center