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Analgesic Effect of Paracetamol, Paracetamol + Codeine, Ibuprofen and Their Combination

Primary Purpose

Pain, Postoperative

Status
Completed
Phase
Phase 4
Locations
Norway
Study Type
Interventional
Intervention
Ibuprofen + Paracetamol
Ibuprofen + Paracetamol + Codeine
Paracetamol + Codeine
Placebo
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Postoperative focused on measuring Paracetamol, Acetaminophen, Ibuprofen, Pain, Postoperative pain, third molar

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of ASA class I in need of surgical removal of impacted third molars and with at least moderate postoperative pain as defined by subjective score on a verbal rating scale after surgical removal of third molars.

Exclusion Criteria:

  • Females stating not suspected or not verified pregnancy after being questioned by investigator.
  • Patients who have used analgesics for 3 days prior to the day of surgery.
  • Patients with known active gastrointestinal bleeding or ulcer.
  • Patients with any known hypersensitivity to NSAIDs.
  • Patients with other drug treatment than contraceptives.
  • Patients smoking before taking the test-drug or during the observation period.
  • Drug addicts or rehabilitated drug addicts.
  • Patients with surgery time exceeding 60 minutes
  • Peroperative complications such as profuse bleeding or perforation to the maxillary sinus requiring additional drug treatment during or after the surgical removal of the third molar.
  • Postoperative complications such as extended bleeding, nausea and regurgitation during the observation period.

Sites / Locations

  • Ullevaal University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Placebo Comparator

Arm Label

Ibuprofen + Paracetamol

Ibuprofen + Paracetamol + Codeine

Paracetamol + Codeine

Placebo

Arm Description

Single oral dose of ibuprofen 400 mg + paracetamol (acetaminophen) 1000 mg

Single oral dose of ibuprofen 400 mg + paracetamol (acetaminophen) 1000 mg + codeine 60 mg

Single oral dose of paracetamol (acetaminophen) 1000 mg + codeine 60 mg

Single oral dose of lactose as placebo

Outcomes

Primary Outcome Measures

Sum pain intensity SPI (0-10 Numerical Rating Scale)

Secondary Outcome Measures

Sum pain intensity difference score (PID)
Overall assessment of efficacy (4-point Verbal Rating Scale)
Adverse effects AE (Specific reporting of AE - type, duration and severity)

Full Information

First Posted
June 15, 2009
Last Updated
March 29, 2016
Sponsor
Ullevaal University Hospital
Collaborators
University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT00921700
Brief Title
Analgesic Effect of Paracetamol, Paracetamol + Codeine, Ibuprofen and Their Combination
Official Title
Analgesic Effect of Ibuprofen 400 mg/Paracetamol 1000 mg, Ibuprofen 400 mg/ Paracetamol 1000 mg/60 mg Codeine, and Paracetamol 1000 mg/Codeine 60 mg: A Single-dose, Randomized, Placebo-controlled and Double-blind Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ullevaal University Hospital
Collaborators
University of Oslo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether the combination of paracetamol (acetaminophen) and other NSAIDs with or without weak opioids can give synergistic analgesic effect.
Detailed Description
Combining paracetamol and other NSAIDs could give a theoretical synergistic analgesic effect according to already known or assumed mechanisms of action. Synergism is defined as an additive or supra-additive effect not achieved by one of the drugs alone. Such synergism is shown in clinical studies between acetaminophen and naproxen in coxarthrosis and rheumatoid arthritis. Later, a significant additive effect of 100 mg diclofenac with 1 g acetaminophen was demonstrated in a dental pain model. One review article conclude that acetaminophen and NSAIDs may be appropriate to combine, and the combination is superior to acetaminophen, but not to NSAIDs alone. This view is contested by another review article which concludes that paracetamol may enhance the analgesic effect when added to an NSAID. In both reviews the authors also state that the clinical trials are too few, with different drug formulations, and different pain models not allowing definite conclusions. There seems to be a need for studies investigating the potential synergistic effects of paracetamol combined with another NSAID displaying similar pharmacokinetic characteristics. To the best of our knowledge no published study has investigated the analgesic effect of the combination of ibuprofen and paracetamol, ibuprofen and paracetamol + codeine versus placebo (i.e. negative control to adjust for possible analgesic placebo effects) and the best standard analgesic treatment (i.e. paracetamol + codeine) as a positive control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative
Keywords
Paracetamol, Acetaminophen, Ibuprofen, Pain, Postoperative pain, third molar

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ibuprofen + Paracetamol
Arm Type
Experimental
Arm Description
Single oral dose of ibuprofen 400 mg + paracetamol (acetaminophen) 1000 mg
Arm Title
Ibuprofen + Paracetamol + Codeine
Arm Type
Experimental
Arm Description
Single oral dose of ibuprofen 400 mg + paracetamol (acetaminophen) 1000 mg + codeine 60 mg
Arm Title
Paracetamol + Codeine
Arm Type
Active Comparator
Arm Description
Single oral dose of paracetamol (acetaminophen) 1000 mg + codeine 60 mg
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Single oral dose of lactose as placebo
Intervention Type
Drug
Intervention Name(s)
Ibuprofen + Paracetamol
Other Intervention Name(s)
Ibuprofen, ATC code: M01A E01, Paracetamol (Acetaminophen), ATC code: N02B E01
Intervention Description
Single oral dose of ibuprofen 400 mg combined with paracetamol (acetaminophen) 1000 mg in gelatine capsules
Intervention Type
Drug
Intervention Name(s)
Ibuprofen + Paracetamol + Codeine
Other Intervention Name(s)
Ibuprofen, ATC code: M01A E01, Paracetamol (Acetaminophen), ATC code: N02B E01, Codeine, ATC code: R05D A04
Intervention Description
Single oral dose of ibuprofen 400 mg combined with paracetamol (acetaminophen) 1000 mg and codeine 60 mg in gelatine capsules
Intervention Type
Drug
Intervention Name(s)
Paracetamol + Codeine
Other Intervention Name(s)
Paracetamol (Acetaminophen), ATC code: N02B E01, Codeine, ATC code: R05D A04
Intervention Description
Single oral dose of paracetamol (acetaminophen) 1000 mg combined with codeine 60 mg in gelatine capsules
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Lactose, CAS No: 63-42-3
Intervention Description
Single oral dose of lactose as placebo in gelatine capsules
Primary Outcome Measure Information:
Title
Sum pain intensity SPI (0-10 Numerical Rating Scale)
Time Frame
6 hours
Secondary Outcome Measure Information:
Title
Sum pain intensity difference score (PID)
Time Frame
6 hours
Title
Overall assessment of efficacy (4-point Verbal Rating Scale)
Time Frame
6 hours
Title
Adverse effects AE (Specific reporting of AE - type, duration and severity)
Time Frame
6 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of ASA class I in need of surgical removal of impacted third molars and with at least moderate postoperative pain as defined by subjective score on a verbal rating scale after surgical removal of third molars. Exclusion Criteria: Females stating not suspected or not verified pregnancy after being questioned by investigator. Patients who have used analgesics for 3 days prior to the day of surgery. Patients with known active gastrointestinal bleeding or ulcer. Patients with any known hypersensitivity to NSAIDs. Patients with other drug treatment than contraceptives. Patients smoking before taking the test-drug or during the observation period. Drug addicts or rehabilitated drug addicts. Patients with surgery time exceeding 60 minutes Peroperative complications such as profuse bleeding or perforation to the maxillary sinus requiring additional drug treatment during or after the surgical removal of the third molar. Postoperative complications such as extended bleeding, nausea and regurgitation during the observation period.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lasse A Skoglund, DDS, DSci
Organizational Affiliation
University of Oslo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Gaute Lyngstad, DDS
Organizational Affiliation
University of Oslo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ullevaal University Hospital
City
Oslo
ZIP/Postal Code
NO-0407
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
8252318
Citation
Seideman P. Additive effect of combined naproxen and paracetamol in rheumatoid arthritis. Br J Rheumatol. 1993 Dec;32(12):1077-82. doi: 10.1093/rheumatology/32.12.1077.
Results Reference
background
PubMed Identifier
8322582
Citation
Seideman P, Samuelson P, Neander G. Naproxen and paracetamol compared with naproxen only in coxarthrosis. Increased effect of the combination in 18 patients. Acta Orthop Scand. 1993 Jun;64(3):285-8. doi: 10.3109/17453679308993626.
Results Reference
background
PubMed Identifier
10613619
Citation
Breivik EK, Barkvoll P, Skovlund E. Combining diclofenac with acetaminophen or acetaminophen-codeine after oral surgery: a randomized, double-blind single-dose study. Clin Pharmacol Ther. 1999 Dec;66(6):625-35. doi: 10.1053/cp.1999.v66.103629001.
Results Reference
background
PubMed Identifier
11878655
Citation
Romsing J, Moiniche S, Dahl JB. Rectal and parenteral paracetamol, and paracetamol in combination with NSAIDs, for postoperative analgesia. Br J Anaesth. 2002 Feb;88(2):215-26. doi: 10.1093/bja/88.2.215.
Results Reference
background
PubMed Identifier
11878654
Citation
Hyllested M, Jones S, Pedersen JL, Kehlet H. Comparative effect of paracetamol, NSAIDs or their combination in postoperative pain management: a qualitative review. Br J Anaesth. 2002 Feb;88(2):199-214. doi: 10.1093/bja/88.2.199.
Results Reference
background
PubMed Identifier
1745622
Citation
Skoglund LA, Skjelbred P, Fyllingen G. Analgesic efficacy of acetaminophen 1000 mg, acetaminophen 2000 mg, and the combination of acetaminophen 1000 mg and codeine phosphate 60 mg versus placebo in acute postoperative pain. Pharmacotherapy. 1991;11(5):364-9.
Results Reference
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Analgesic Effect of Paracetamol, Paracetamol + Codeine, Ibuprofen and Their Combination

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