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Study of Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)for Treatment of Post Operative Nausea and Vomiting

Primary Purpose

Nausea, Vomiting

Status
Unknown status
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)
Metoclopramide hydrochloride monohydrate
Sponsored by
CM Chungmu Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Nausea focused on measuring post operative nausea and vomiting, Trimebutine Maleate

Eligibility Criteria

undefined - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • post arthroscopic cuff repair patient previously diagnosed with small to large rotator cuff tear thru MRI

Exclusion Criteria:

  • above 70 years old
  • massive rotator cuff tear

Sites / Locations

  • Chungmu General HopsitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Trimebutine Maleate 300 mg Tab

Metoclopramide hydrochloride monohydrate 8.46 mg/2ml/A

Arm Description

A single dose of NEWBUTIN SR 300 mg Tab will be given orally one hour prior to the said operation time and another 300 mg orally as soon as the patient wakes post operatively.

Anti-emetic medication protocol of Chungmu Hospital includes MACPERAN (Metoclopramide hydrochloride monohydrate 8.46 mg/2ml/A)thru IV twice in a day

Outcomes

Primary Outcome Measures

Severity of nausea after taking Trimebutine Maleate as a prophylactic medication
The severity of nausea will be graded on a four-point scale. 0- no nausea (can do all tasks). 1- mild nausea (can talk and answer questions appropriately,sit, stand but can't walk). 2- moderate nausea (can talk and but answer questions inappropriately, sit but can't stand and walk). 3- severe nausea (don't talk and answer questions, prefers lying down, cannot sit, stand and walk).

Secondary Outcome Measures

Frequency of PONV after taking Trimebutine Maleate as a prophylactic medication
Frequency is how often the patient experienced the episodes of nausea and vomiting in a given time period.

Full Information

First Posted
October 31, 2013
Last Updated
November 8, 2013
Sponsor
CM Chungmu Hospital
Collaborators
Korea United Pharm. Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01984931
Brief Title
Study of Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)for Treatment of Post Operative Nausea and Vomiting
Official Title
Trimebutine Maleate (NEWBUTIN SR 300 mg Tab) as a Prophylactic Anti-emetic Drug for Patients Who Underwent Arthroscopic Rotator Cuff Repair: a Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
CM Chungmu Hospital
Collaborators
Korea United Pharm. Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will determine if giving Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)orally will be effective as a prophylactic anti-emetic drug for patients who underwent arthroscopic rotator cuff repair under general anesthesia.
Detailed Description
The patients will be divided in two groups using a computer generated randomization software. The first will be the MACPERAN group (controlled) and the other will be the NEWBUTIN group (variable). The controlled group will be treated with post-operative regimen in accordance with the standard protocol of the Chungmu Hospital, MACPERAN(Metoclopramide hydrochloride monohydrate 8.46 mg/2ml/A) thru IV twice in a day while the variable group will be given a single dose of NEWBUTIN SR 300 mg Tab orally one hour prior to the said operation time and another 300 mg orally as soon as the patient wakes post operatively. A clinical research coordinator will monitor the patient until 48 hours post-operative. First time frame will be from 0-2 hours once patient is transferred to the ward followed by 2 hours to 24 hours and 24-48 hours post ward transfer. All patients will be assessed using the simplified risk score of Apfel et al. to determine who have the risk factors for PONV. The episodes of nausea and vomiting will be recorded taking note of its intensity and frequency on the said three time frames. Nausea is defined as a subjectively unpleasant sensation associated with an awareness of the urge to vomit; vomiting is defined as the forceful expulsion of gastric contents through the mouth. As retching is similar to vomiting in all aspects, except for the expulsion of gastric contents, it was considered as vomiting. The efficacy of anti-emetic medication (NEWBUTIN 300 mg/tab) will be assessed by monitoring the frequency and severity of nausea, vomiting, and PONV (which was regarded as the primary outcome). The severity of nausea will be graded on a four-point scale, where 0= no nausea, 1= mild nausea, 2= moderate nausea, and 3= severe nausea.Then the frequency will be assessed by monitoring how often the patient experienced these episodes (nausea and vomiting)during the said time frames.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nausea, Vomiting
Keywords
post operative nausea and vomiting, Trimebutine Maleate

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trimebutine Maleate 300 mg Tab
Arm Type
Experimental
Arm Description
A single dose of NEWBUTIN SR 300 mg Tab will be given orally one hour prior to the said operation time and another 300 mg orally as soon as the patient wakes post operatively.
Arm Title
Metoclopramide hydrochloride monohydrate 8.46 mg/2ml/A
Arm Type
Active Comparator
Arm Description
Anti-emetic medication protocol of Chungmu Hospital includes MACPERAN (Metoclopramide hydrochloride monohydrate 8.46 mg/2ml/A)thru IV twice in a day
Intervention Type
Drug
Intervention Name(s)
Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)
Other Intervention Name(s)
•Antinime, •Cineprac, •Colixane B (Trimebutine and Bromazepam), •Colixane Prokin (Trimebutine and Mosapride), •Colixane, •Colonix B (Trimebutine and Bromazepam), •Colonix, •Colospasmyl, •Colperin, •Crobutin, •Debricol, •Debridat, •Débridat, •Eumotrix, •Ibuproct (Trimebutine and Ruscogenin), •Ibutin, •Libertrim, •Libertrim Pediátrico (pediatric), •Libertrim SDP (Trimebutine and Simeticone), •Libertrim SII (Trimebutine and Simeticone), •Muvett, •Polybutine, •Prescol, •Proctolog (Trimebutine and Ruscogenin), •Promebutin, •Ruscolog (Trimebutine and Ruscogenin), •Tribux, •Trimebutin, •Trimebutina Genfar, •Trimebutina La Santé, •Trimebutina, •Trimebutino Andromaco, •Trimedine, •Trimegam, •Trimet, •Altrip, •Apo-Trimebutine, •Biorgan B (Trimebutine and Bromazepam), •Biorgan, •Bumetin, •Butikinon, •Cerekinon, •Cerenamelin, •Colobutine, •Colypan, •Debretin, •Debricalm, •Debridat AP, •Debridat B (Trimebutine and Bromazepam), •Debridat Fort, •Debrum (Trimebutine and Medazepam), •Derispan, •Digerent, •Diway, •Dolpic, •Eumotil, •Eumotil-S (Trimebutine and Simeticone), •Eumotil-T (Trimebutine and Bromazepam), •Eutransil, •Fenatrop, •Garapepsin, •Gaspat, •Gismotal, •Liement, •Mebucolon, •Mebutit, •Miopropan, •Modulon, •Mustrick, •Muvett S (Trimebutine and Simeticone), •Newbutin SR, •Ni Wei Fu, •Pelkysil, •Pilemain, •Polibutin, •Recutin, •Rekelat, •Rui Jian, •Sakion, •Selumito, •Shuang Di, •Spabutine, •Spamoin, •Supeslone, •Sutent, •Tarabutine, •Tefmetin, •Tidomel, •Timotor, •Transacalm, •Tribudat Forte, •Tribudat, •Tributin, •Tricin, •Tridat, •Trienter, •Trim, •Trimebutin Maleate Taiyo, •Trimebutina Angenerico, •Trimebutina Colmed, •Trimebutina maleato, •Trimebutina MK, •Trimébutine Actavis, •Trimébutine Almus, •Trimébutine ALS, •Trimébutine Arrow, •Trimébutine Biogaran, •Trimébutine CristerS, •Trimébutine EG, •Trimébutine Evolugen, •Trimébutine Isomed, •Trimébutine maléate RPG, •Trimébutine Mylan, •Trimébutine Pfizer, •Trimébutine Qualimed, •Trimébutine Ranbaxy, •Trimébutine Ratio, •Trimébutine Ratiopharm, •Trimébutine Sandoz, •Trimébutine Teva, •Trimébutine Zentiva, •Trimébutine Zydus, •Trimebutino Maleato, •Trimedat, •Trishi, •VeM, •Yuan Sheng Li Wei
Intervention Description
Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)is a noncompetitive spasmolytic agent. It possesses moderate opiate receptor affinity and has marked anti-serotonin activity especially on'M' receptors. A single dose of NEWBUTIN SR 300 mg Tab orally will be given one hour prior to the said operation time and another 300 mg orally as soon as the patient wakes post operatively.
Intervention Type
Drug
Intervention Name(s)
Metoclopramide hydrochloride monohydrate
Primary Outcome Measure Information:
Title
Severity of nausea after taking Trimebutine Maleate as a prophylactic medication
Description
The severity of nausea will be graded on a four-point scale. 0- no nausea (can do all tasks). 1- mild nausea (can talk and answer questions appropriately,sit, stand but can't walk). 2- moderate nausea (can talk and but answer questions inappropriately, sit but can't stand and walk). 3- severe nausea (don't talk and answer questions, prefers lying down, cannot sit, stand and walk).
Time Frame
0-48 hours post rotator cuff repair
Secondary Outcome Measure Information:
Title
Frequency of PONV after taking Trimebutine Maleate as a prophylactic medication
Description
Frequency is how often the patient experienced the episodes of nausea and vomiting in a given time period.
Time Frame
0-48 hours post rotator cuff repair

10. Eligibility

Sex
All
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: post arthroscopic cuff repair patient previously diagnosed with small to large rotator cuff tear thru MRI Exclusion Criteria: above 70 years old massive rotator cuff tear
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sang Hoon Lhee, MD, PhD
Phone
+82 (2) 2068/4525
Email
cmirb@naver.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paolo Alan B Tabar, MD
Organizational Affiliation
International Education Center of Shoulder, Elbow Surgery: Chungmu Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chungmu General Hopsital
City
Seoul
State/Province
Yeongdeungpo-gu
ZIP/Postal Code
150-034
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sang Hoon Lhee, MD, Phd
Phone
+82 (2) 2068/4525
Email
cmirb@naver.com
First Name & Middle Initial & Last Name & Degree
Paolo Alan B Tabar, MD

12. IPD Sharing Statement

Learn more about this trial

Study of Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)for Treatment of Post Operative Nausea and Vomiting

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