Botulinum Toxin Injection in Patients Undergoing Hemorrhoidectomy-A Prospective Randomized Study
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- STATUS
- Recruiting
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- participants needed
- 60
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- sponsor
- Tri-Service General Hospital
Summary
This is a prospective, randomized study, which anticipatedly recruited 60 patients in the outpatient department who need hemorrhoidectomy from January 2019 to December 2019. After obtaining those patients' consent in the clinic, they were randomly assigned to two groups at a 1:1 ratio using a computer-generated list of random numbers (Microsoft Excel). One group received Botulinum toxin injection during the outpatient clinic one week before the operation(experimental group, EG), and the other group received injection during the operation(control group, CG). The two groups were compared for the influence of postoperative pain control and wound healing rate.
Details
Condition | The Influence of Timing of Botulinum Toxin Injection on Postoperative Pain Control |
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Age | 20years - 80years |
Treatment | Botulinum toxin type A |
Clinical Study Identifier | NCT04485780 |
Sponsor | Tri-Service General Hospital |
Last Modified on | 5 August 2020 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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