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Lidocaine vs. tramadol vs. placebo wound infiltration for post-cesarean section pain relief: a randomized controlled trial

This article has been retracted. Retraction note.
  • Ahmed Hussein , Haitham Torky ORCID logo EMAIL logo , Rania Aly , Mazen Abdel-Rasheed , Ashraf El-Baz , Hossam Mahmoud , Sileem Sileem , Mahmoud Badawy , Zainab Sayd , Osama Dief , Ahmed Elsadek , Heba Marie and Ashraf Abo-Louz
Published/Copyright: May 10, 2022

Abstract

Objectives

In low-income settings, postoperative pain relief could be challenging as a high patient/nurse ratio limits pain assessment and adequate analgesics administration. The multi-center prospective double-blinded parallel randomized controlled trial was done to compare lidocaine, tramadol, and placebo (saline) intraoperative wound infiltration to relieve post-cesarean section wound pain during the first 24 h.

Methods

Ninety-nine cases were equally randomized into three groups, each containing 33 pregnant women undergoing cesarean section under general anesthesia. During operation, the wound was infiltrated subcutaneously with 20 mL of 2% lidocaine solution in the first group, 2 mg/kg tramadol in the second group, and saline in the third group. The primary outcome was to assess the postoperative pain at 2, 4, 6, 12, and 24 h by the Yes-No-Don’t Know (YNDK) Scale, while the secondary outcome was to assess the need for further postoperative analgesia.

Results

Wound infiltration with lidocaine or tramadol was effective in pain relief, and both were superior to placebo. Wound infiltration with tramadol was superior to lidocaine in pain relief at 2 h and up to 24 h.

Conclusions

Wound infiltration with tramadol has a more prolonged pain relief effect than lidocaine in post-cesarean section pain relief in patients performing cesarean section under general anesthesia lasting up to 24 h, and both are superior to placebo in pain relief.


Corresponding author: Haitham Torky, Professor, Department of Obstetrics & Gynecology, October 6th University, Giza, Egypt, Phone: +20 1001230161, Fax: +20 225240066, E-mail:

  1. Research funding: None declared.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The local Institutional Review Board approved the study.

  6. Trial registration: The Pan-African Clinical trial registry PACTR201711002756172.

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Received: 2021-11-21
Accepted: 2022-04-11
Published Online: 2022-05-10
Published in Print: 2022-10-26

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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