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Randomized Controlled Trial Comparative Study Clinical Trial
Efficacy of preemptive analgesia for wound pain after laparoscopic operations in infertile women: a randomised, double-blind and placebo control study.
- K W Lam, T C Pun, E H Y Ng, and K S Wong.
- Department of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong.
- BJOG. 2004 Apr 1; 111 (4): 340-4.
ObjectiveTo compare preemptive analgesia and preclosure analgesia in reducing wound pain after laparoscopic operation.DesignRandomised, double-blind and placebo control.SettingUniversity referral centre.PopulationInfertile women undergoing diagnostic laparoscopy with or without additional procedures.MethodsOne hundred and forty-four women were randomised to receive 10 mL of 1% lignocaine at the surgical sites before incision and 10 mL of normal saline before closure of incision (the preemptive group), saline before incision and lignocaine before closure of incision (the preclosure group) and saline at the surgical sites both before incision and closure of incision (the placebo group).Main Outcome MeasuresPost-operative wound pain measured by linear visual analogue scale and amount of analgesic use.ResultsThe women in the preclosure group had significantly lower pain scores at 2, 4 and 24 hours than those in the placebo group, whereas the women in the preemptive group only showed significantly lower pain scores at 2 hours than the placebo group. The pain score at 24 hours in the preclosure group was significantly lower than that in the preemptive group. There was no significant difference in the post-operative analgesic requirement among the three groups.ConclusionThe preclosure analgesia is better than preemptive analgesia and no analgesia in reducing post-operative wound pain.
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