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Dexketoprofen Trometamol in Postoperative Endodontic Pain (DTPEP)

Primary Purpose

Irreversible Pulpitis

Status
Completed
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Dexketoprofen trometamol
Ibuprofen
PLACEBO
Sponsored by
Daniel Chavarría Bolaños
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Irreversible Pulpitis focused on measuring pain, symptomatic irreversible pulpitis, postoperative dental pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Subjects aged 18 years and older with moderate-to-severe dental pain assessed by numerical rating scale (NRS) associated with irreversible pulpitis.

Exclusion Criteria:

  • • Female pregnant or breastfeeding

    • Used pain relievers or anti-inflammatory drugs within 24 hours preceding emergency endodontic treatment
    • Have any significant medical condition
    • Taking any medications for anxiety, depression or schizophrenia
    • Have a history of hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs)

Sites / Locations

  • Endodontics Master Degree program, Dentistry Faculty, San Luis Potosi University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

dexketoprofen trometamol

IBUPROFEN

PLACEBO

Arm Description

Administration of 25mg of Dexketoprofen Trometamol, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed

Administration of 600mg of Ibuprofen, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed

4 doses of sugar pills, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed

Outcomes

Primary Outcome Measures

post operative pain measurement in symptomatic irreversible pulpitis, after multiple doses of dexketoprofen trometamol
Using a visual analogue scale, each patient is asked to inform the researcher team about postoperative pain levels at 1, 8, 16, 24, 48 and 72 hours after pulpotomy procedure as emergency clinical manage of endodontic pain in irreversible pulpitis cases. Patients will be asked to take multiple doses of either Dexketoprofen Trometamol 25mg, Ibuprofen 600mg or placebo pills. Also, aspects like local anesthetic effect duration and local/systemic side effects will be monitored. Each patient will have a personal file to record the information during each period (1, 8, 16, 24, 48 and 72 hours )

Secondary Outcome Measures

Duration of the activity of the analgesic treatment
The duration of the effect of each drug will be recorded

Full Information

First Posted
March 7, 2014
Last Updated
May 6, 2014
Sponsor
Daniel Chavarría Bolaños
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1. Study Identification

Unique Protocol Identification Number
NCT02086097
Brief Title
Dexketoprofen Trometamol in Postoperative Endodontic Pain
Acronym
DTPEP
Official Title
Effectiveness of Dexketoprofen Trometamol in the Management of Postoperative Endodontic Pain. Controlled Clinical Trial of Multiple Doses
Study Type
Interventional

2. Study Status

Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Daniel Chavarría Bolaños

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to investigate the analgesic efficacy of multiple doses of Dexketoprofen Trometamol 25 mg on postoperative pain following emergency endodontic treatment in teeth with irreversible pulpitis, using as control Ibuprofen 600 mg and a placebo group. Hypothesis: Dexketoprofen trometamol when administered in multiple doses produces a greater effect to control postoperative pain after treating symptomatic irreversible pulpitis; in patients undergoing pulpotomy as an emergency procedure
Detailed Description
Pain management is an integral part of Endodontics, according to previously published results, pulp therapy and endodontic treatment induce postoperative pain more frequently than other dental procedures. The prevalence of postoperative pain has been reported in 3-58% of cases, a positive association has been demonstrated between postoperative pain and the presence of apprehension and preoperative pain. Although the incidence of moderate pain decreases within 1 day and substantially to minimal levels in 7 days after the endodontic treatment, severe postoperative pain occurs during the first 24 h. Some drugs can prevent the production of inflammatory mediators involved in producing pain, such as prostaglandins. Prostaglandin tissue levels are associated with patient reports of pain, and therefore, nonsteroidal anti-inflammatory drugs (NSAID's) may be key drugs for inflammatory pain abatement. NSAIDs are widely available, and they have been reported to be effective in managing endodontic pain. Ibuprofen is one of the most frequently used NSAIDs for control of postoperative pain associated with root canal treatment, and it has good efficacy and safety. However an alternative treatment is Dexketoprofen Trometamol, a non-selective nonsteroidal anti-inflammatory drug, and a single isomer (S(+)-enantiomer) of ketoprofen formulated as trometamol salt. Dexketoprofen trometamol has been demonstrated to be effective in the treatment of acute pain. The purpose of the study is assess the analgesic efficacy of multiple doses of Dexketoprofen Trometamol 25 mg on postoperative pain following emergency endodontic treatment in teeth with irreversible pulpitis This study was designed as a double-blind, randomised, placebo-controlled clinical trial. Following the guidelines suggested by CONSORT group for planning and reporting clinical trials. The ethics committee of the faculty of Dentistry approved the study design. All of the subjects will be informed of the possible risk of endodontic therapy and experimental treatments and will sign institutionally approved consents forms. In total, 87 patients will be included in this study. The simple size calculation was performed with a type error of 0.05 and statistical power of 80% on the basis of report of the analgesic efficacy of Dexketoprofen Trometamol 25 mg vs Ibuprofen 600 mg after their administration in patients subject to oral surgery. All of the subjects voluntarily will presented at the postgraduate endodontics clinic of the Faculty of Dentistry at San Luis Potosí University. The select subjects will have a diagnosis of symptomatic irreversible pulpitis. Pain will be scored using numerical rating scale, this is a 11 point scale where the end points are the extremes of no pain and pain as bad as it could be, or worst pain. Accordingly, no pain corresponded with 0, mild pain with 1-3, moderate pain with 4-6, and severe pain 7 and above.7 After the endodontic emergency treatment, patients will be randomly divided into three groups of 27 patients each. A control group will receive multiple doses of placebo and 2 experimental groups receive multiple dose of ibuprofen (600 mg) and Dexketoprofen trometamol (25 mg). The first dose of medication is given once the procedure is completed, the following doses will be taken every 8 hours to cover a total of 24 hours. Patients will be monitored to assess the therapeutic effect at different time intervals, 1,8,16,24,48 and 72 hours using numerical rating scale. If the analgesic efficacy is not achieved Supradol (Ketorolac 30 mg) or Zaldiar (Paracetamol 325mg/Tramadol 37.5 mg) will be taken as rescue medication.Any adverse events or symptoms will be recorded. Statistics Normal distribution will be tested by the Student's-t test or mann-whitney U test. A non -parametric chi-squared test was performed to identify statistically significant differences between the groups; the level of significance was set at p<0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irreversible Pulpitis
Keywords
pain, symptomatic irreversible pulpitis, postoperative dental pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
dexketoprofen trometamol
Arm Type
Experimental
Arm Description
Administration of 25mg of Dexketoprofen Trometamol, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed
Arm Title
IBUPROFEN
Arm Type
Active Comparator
Arm Description
Administration of 600mg of Ibuprofen, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed
Arm Title
PLACEBO
Arm Type
Placebo Comparator
Arm Description
4 doses of sugar pills, 1 pill right after clinical procedure, the other 3 every 8 until the 24 hours administration period is completed
Intervention Type
Drug
Intervention Name(s)
Dexketoprofen trometamol
Other Intervention Name(s)
Miracox (Stein Labs), CODE: 00176101
Intervention Description
25m of dexketoprofen (oral intake) every 8 hours
Intervention Type
Drug
Intervention Name(s)
Ibuprofen
Other Intervention Name(s)
Ibuprofen Stein, CODE: 00065104
Intervention Description
600 mg of Ibuprofen (Oral Intake) every 8 hours
Intervention Type
Drug
Intervention Name(s)
PLACEBO
Other Intervention Name(s)
PLAC
Intervention Description
INACTIVE SUGAR PILLS
Primary Outcome Measure Information:
Title
post operative pain measurement in symptomatic irreversible pulpitis, after multiple doses of dexketoprofen trometamol
Description
Using a visual analogue scale, each patient is asked to inform the researcher team about postoperative pain levels at 1, 8, 16, 24, 48 and 72 hours after pulpotomy procedure as emergency clinical manage of endodontic pain in irreversible pulpitis cases. Patients will be asked to take multiple doses of either Dexketoprofen Trometamol 25mg, Ibuprofen 600mg or placebo pills. Also, aspects like local anesthetic effect duration and local/systemic side effects will be monitored. Each patient will have a personal file to record the information during each period (1, 8, 16, 24, 48 and 72 hours )
Time Frame
1 observation after 72 hours of emergency clinical procedure (Pulpotomy) for pain management
Secondary Outcome Measure Information:
Title
Duration of the activity of the analgesic treatment
Description
The duration of the effect of each drug will be recorded
Time Frame
observation periods of 1, 8, 16, 24, 48 AND 72 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects aged 18 years and older with moderate-to-severe dental pain assessed by numerical rating scale (NRS) associated with irreversible pulpitis. Exclusion Criteria: • Female pregnant or breastfeeding Used pain relievers or anti-inflammatory drugs within 24 hours preceding emergency endodontic treatment Have any significant medical condition Taking any medications for anxiety, depression or schizophrenia Have a history of hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gisela Rodríguez, DDS
Organizational Affiliation
Universidad Autonoma San Luis Potosi
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Amaury J Pozos-Guillen, PhD
Organizational Affiliation
Universidad Autonoma San Luis Potosi
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Daniel Chavarria, PhD
Organizational Affiliation
Universidad Autonoma San Luis Potosi
Official's Role
Study Director
Facility Information:
Facility Name
Endodontics Master Degree program, Dentistry Faculty, San Luis Potosi University
City
San Luis Potosi
ZIP/Postal Code
78290
Country
Mexico

12. IPD Sharing Statement

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Dexketoprofen Trometamol in Postoperative Endodontic Pain

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