PoPuLAR: Intravenous or Intra-abdominal Local Anesthetics for Postoperative Pain Management.

Sponsor
Örebro University, Sweden (Other)
Overall Status
Completed
CT.gov ID
NCT01492179
Collaborator
(none)
60
1
3
19
3.2

Study Details

Study Description

Brief Summary

Local anesthetics (LA) are increasingly used for postoperative pain management. Speicifically, several studies have found benefit of LA injected intra-abdominally following abdominal hysterectomy. However, it remains unclear whether the pain relief seen is due to local anesthetic mechanisms within the abdominal cavity or through systemic absorption. The aim of this study is to assess whether lidocaine administered intravenously has similar analgesic efficacy as the same dose administered intra-abdominally in patients undergoing abdominal hysterectomy. All patients would have rescue analgesia using the patient controlled analgesia (PCA) pump with morphine in order to achieve adequate pain management during 24 h.

Condition or Disease Intervention/Treatment Phase
  • Drug: Normal saline
  • Drug: Intravenous Lidocaine
  • Drug: Intra-abdominal Lidocaine
Phase 4

Detailed Description

Abdominal hysterectomy with or without salipingo-oophorectomy is associated with moderate-severe postoperative pain. Poor pain control in the postoperative period can lead to increased postoperative morbidities and poor quality of life. Furthermore, an emerging clinical literature suggests that acute pain may rapidly evolve into chronic pain if poorly treated. A meta-analysis of the literature found that > 30% patients had chronic pain one year after abdominal hysterectomy (5). Therefore, efficient postoperative pain management is imperative for the patient and is one of the new pain management standards recommended recently.

Local anesthetics (LA) have been infiltrated subcutaneously, infused intra-abdominally, as well as injected into the peritoneal cavity as a single dose at the end of the operation following abdominal hysterectomy with variable effects. When injected as a single dose, analgesia is limited to approximately 2-4 hours due to the short duration of action of local anesthetics. In one recent study, the authors used a catheter inserted intra-abdominally and local anesthetic or placebo infusion into the abdominal cavity for 24 h postoperatively and found a reduction in postoperative analgesic requirements by 40% during 4-24 h. In another study, the investigators found that LA injected intermittently intra-abdominally resulted in better pain relief compared to intra-abdominal infusions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Comparison Between Continuous Infusion vs. Patient Controlled Intraabdominal Injection of Local Anesthetics for Treatment of Postoperative Pain After Abdominal Hysterectomy. A Randomized, Double-blind Study.
Study Start Date :
Nov 1, 2011
Actual Primary Completion Date :
Jun 1, 2013
Actual Study Completion Date :
Jun 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Intravenous Lidocaine

Intravenous lidocaine would be administered as an infusion for pain management both intra- and post-operatively.

Drug: Intravenous Lidocaine
Standardized infusion of lidocaine during 24 h. 100 mg bolus and 50 mg/h during 24 h would be administered.
Other Names:
  • Xylocaine 5 mg/ml
  • Active Comparator: Intra-abdominal Lidocaine

    Lidocaine would be administered intermittently, once each hour intra-abdominally for postoperative pain management.

    Drug: Intra-abdominal Lidocaine
    Lidocaine 5 mg/ml; 100 mg would be administered intraoperatively intra-abdominally and subsequently 50 mg/h as intermittent injection intra-abdominally during 24 h
    Other Names:
  • Xylocaine 5 mg/ml
  • Placebo Comparator: Normal saline

    Normal saline would be administered intra-abdominally and intravenously in the same patient. Rescue analgesia in the form of morphine (PCA) would be used for pain management.

    Drug: Normal saline
    Normal saline would be administered intravenously and intra-abdominally.

    Outcome Measures

    Primary Outcome Measures

    1. Morphine consumption [0 - 24 h postoperatively]

      Total rescue morphine consumption during 0 - 24 h would be the primary endpoint

    Secondary Outcome Measures

    1. Postoperative pain [4 h postoperatively]

      Postoperative pain measured on the numeric rating scale (0 - 10) would be measured at 4 h

    2. Plasma concentration of lidocaine [24 h]

      The plasma concentration of LA lidocaine would be analysed at 24 h in order to assess whether the LA absorption from the abdomen is similar to that administered intravenously.

    3. Length of Hospital stay [1-5 days]

      The time to discharge home would be assessed using standardized criteria for home discharge.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 75 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • ASA 1-2

    • 30 - 75 yrs

    • Informed consent

    • 50 - 100 kg

    Exclusion Criteria:
    • Allergy to LA

    • Chronic pain

    • Major liver/kidney insufficiency

    • AV Block 1-2 Participation in another clinical trial

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Örebro University Hospital Örebro Sweden 701 85

    Sponsors and Collaborators

    • Örebro University, Sweden

    Investigators

    • Study Director: Kjell Axelsson, MD, PhD, Örebro University Hospital, Örebro, Sweden

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Anil Gupta, Associate Professor, Örebro University, Sweden
    ClinicalTrials.gov Identifier:
    NCT01492179
    Other Study ID Numbers:
    • 20111212
    First Posted:
    Dec 14, 2011
    Last Update Posted:
    May 28, 2014
    Last Verified:
    May 1, 2014
    Keywords provided by Anil Gupta, Associate Professor, Örebro University, Sweden
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 28, 2014