Intraperitoneal Tramadol Versus Dexmedetomedine for Analgesia After Abdominal Laparoscopic Cancer Surgeries

Sponsor
National Cancer Institute, Egypt (Other)
Overall Status
Completed
CT.gov ID
NCT04813016
Collaborator
(none)
100
1
4
14
7.1

Study Details

Study Description

Brief Summary

Multiple modalities for postoperative analgesia after laparoscopic procedures has been used, of them intraperitoneal route (IP) was used to decrease the analgesic requirements. Both early and late bupivacaine and tramadol versus bupivacaine and dexmedetomedine will be tried to choose which is having a better analgesic profile.

Condition or Disease Intervention/Treatment Phase
  • Drug: Tramal 1
  • Drug: Tramal 2
  • Drug: Dexmedetomidine 1
  • Drug: dexmedetomidine 2
Phase 2/Phase 3

Detailed Description

Recently laparoscopic procedures have become popular and familiar to both surgeons and anesthetists. They have many advantages such as rapid postoperative recovery, low postoperative complication rates, early mobilization, and early home discharge; consequently reduce hospital stay and costs. Although previous studies have been shown that laparoscopy is associated with less pain than laparotomy, it is not totally pain free. Some laparoscopic procedures for abdominal cancer surgeries has shown that there may be more intense pain and greater analgesic requirements in the immediate postoperative period than after open laparotomy.

Thoroughly understanding the difference of pain generators in laparotomy than in laparoscopy gave some ideas helping in the control of each of them. While laparotomy results mainly in parietal pain, visceral pain remains predominantly in patients after laparoscopic surgeries resulting from the stretching of intra-abdominal cavity, peritoneal inflammation and phrenic nerve irritation caused by residual carbon dioxide in the peritoneal cavity resulting in postoperative abdominal and shoulder pain after laparoscopy. Hence, Intraperitoneal (IP) administration of some drugs can be effective for pain relief after laparoscopic surgery. The results have been variable as the published studies are heterogeneous and often lack appropriate controls. For that, no definitive conclusion can yet be made regarding its value and effectiveness.

The α2-adrenergic agonist provides excellent sedation, anxiolysis, analgesia and sympatholysis. Of them, dexmedetomidine has become one of the frequently used drugs in anaesthesia aiming to its hemodynamic, sedative, anxiolytic, analgesic, neuroprotective and anaesthetic sparing effect. In addition, the high selectivity of dexmedetomidine to α2- receptors favored its widespread use in regional anaesthesia practice and local nerve blocks techniques.

As noradrenergic neurons descending through the dorso-lateral funiculus from the brainstem to the dorsal horn significantly contribute in the modulation of pain by controlling impulse transmission (descending inhibitory pathway). Adrenergic agonists, such as dexmedetomedine, possess significant antinociceptive activity by a central action on the brainstem and a spinal action on the substantia gelatinosa of the dorsal horn.

Tramadol is a synthetic opioid pain medication used to treat moderate to moderately severe pain. It exerts its analgesic effects through a variety of different targets on the noradrenergic, serotoninergic and opioid receptors systems. It also exists as a racemic mixture, the positive enantiomer inhibits serotonin reuptake while the negative enantiomer inhibits noradrenaline re-uptake, by binding to and blocking the transporters. Finally, tramadol has also been shown to act as a serotonin releasing agent. Both enantiomers of tramadol are agonists of the μ-opioid receptor and its M1 metabolite, O-demethylate, which is also a μ-opioid receptor agonist but is 6 times more potent than tramadol itself. All these effects work synergistically to induce analgesia.

The aim of this study is to examine and compare the effect of both early and late intraperitoneal bupivacaine/tramadol and bupivacaine/dexmedetomedine analgesia on the effectiveness of postoperative analgesia and the requirement of postoperative rescue analgesics after laparoscopic surgery for abdominal cancer surgeries.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Treatment
Official Title:
Comparative Study Between Intraperitoneal Administration of Either Bupivacaine and Tramadol Versus Bupivacaine and Dexmedetomedine for Analgesia After Abdominal Laparoscopic Cancer Surgeries. A Prospective Randomized Pilot Study
Actual Study Start Date :
Mar 1, 2021
Actual Primary Completion Date :
Apr 30, 2022
Actual Study Completion Date :
May 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Early tramal/bupivacaine

patients received 50 ml of isotonic aqueous solution (PH 7.45) of tramadol 150mg mixed with bupivacaine 0.25% immediately before creation of a pneumoperitoneum and placement of the first two trocars before starting the surgery.

Drug: Tramal 2
Late intraperitoneal injection of tramal and bupivacaine
Other Names:
  • Late tramal
  • Drug: Dexmedetomidine 1
    Early intraperitoneal injection of dexmedetomidine and bupivacaine
    Other Names:
  • Early Dexmedetomidine
  • Drug: dexmedetomidine 2
    Late intraperitoneal injection of dexmedetomedine and bupivacaine
    Other Names:
  • Late Dexmedetomidine
  • Active Comparator: Late tramal/bupivacaine

    patients received 50ml of isotonic aqueous solution (PH 7.45) of tramadol 150mg mixed with bupivacaine 0.25% after completion of surgery and before trocars removal.

    Drug: Tramal 1
    Early intraperitoneal injection of tramal and bupivacaine
    Other Names:
  • Early tramal
  • Drug: Dexmedetomidine 1
    Early intraperitoneal injection of dexmedetomidine and bupivacaine
    Other Names:
  • Early Dexmedetomidine
  • Drug: dexmedetomidine 2
    Late intraperitoneal injection of dexmedetomedine and bupivacaine
    Other Names:
  • Late Dexmedetomidine
  • Active Comparator: Early dexmedetomedine/bupivacaine

    patients received 50ml of isotonic aqueous solution (PH 7.45) of dexmedetomedine(1µ/kg) mixed with bupivacaine 0.25% before creation of a pneumoperitoneum and placement of the first two trocars before the start of surgery.

    Drug: Tramal 1
    Early intraperitoneal injection of tramal and bupivacaine
    Other Names:
  • Early tramal
  • Drug: Tramal 2
    Late intraperitoneal injection of tramal and bupivacaine
    Other Names:
  • Late tramal
  • Drug: dexmedetomidine 2
    Late intraperitoneal injection of dexmedetomedine and bupivacaine
    Other Names:
  • Late Dexmedetomidine
  • Active Comparator: Late dexmedetomedine/bupivacaine

    patients received 50ml of isotonic aqueous solution (PH 7.45) of dexmedetomedine(1µ/kg) mixed with bupivacaine 0.25% after completion of surgery and before trocars removal.

    Drug: Tramal 1
    Early intraperitoneal injection of tramal and bupivacaine
    Other Names:
  • Early tramal
  • Drug: Tramal 2
    Late intraperitoneal injection of tramal and bupivacaine
    Other Names:
  • Late tramal
  • Drug: Dexmedetomidine 1
    Early intraperitoneal injection of dexmedetomidine and bupivacaine
    Other Names:
  • Early Dexmedetomidine
  • Outcome Measures

    Primary Outcome Measures

    1. The degree of pain [24 hours]

      measurement of VAS

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • ASA II or III.

    • Age 18 to 65 years.

    • Elective surgeries

    Exclusion Criteria:
    • Patients with severe hepatic (more than child c), renal (known CKD)and cardiac (known IHD) troubles.

    • Patients with extensive intraperitoneal adhesions.

    • Patients with a history of drug or analgesic abuse.

    • Known drug allergy or indigestion.

    • Intraoperative lavage of more than 500ml.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Cancer Institute Cairo Egypt 11796

    Sponsors and Collaborators

    • National Cancer Institute, Egypt

    Investigators

    • Principal Investigator: Ehab H Gendy, MD, Assistant Professor of Anesthesia, intensive care and pain releif

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Ehab Hanafy Shaker, Assistant professor of Anesthesia, intensive care and pain releif, National Cancer Institute, Egypt
    ClinicalTrials.gov Identifier:
    NCT04813016
    Other Study ID Numbers:
    • intraperitoneal analgesia
    First Posted:
    Mar 24, 2021
    Last Update Posted:
    Jun 2, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 2, 2022