Clinical Trials Directory

Trials / Completed

CompletedNCT04578483

Postoperative Pain Management of Therapeutic Surgery: a Prospective, Observational Cohort Study.

Status
Completed
Phase
Study type
Observational
Enrollment
634 (actual)
Sponsor
China Medical University Hospital · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Poor management of post-operative acute pain can contribute to medical complications including pneumonia, deep vein thrombosis, infection and delayed healing, as well as the development of chronic. In contrast, appropriate pain control is capable of reducing the postoperative complications, preventing the development of chronic pain, and improving the quality of life. The workloads of medical staffs and health care cost are subsequently decreased. Recently, a lot of analgesic methods have been developed and used in clinical practice, such as patient-controlled analgesia, ultrasound-guided long-term analgesia and multimodal analgesia. This study is aimed to investigate the effect of dinalbuphine sebacate, a long-acting analgesic, in postoperative pain management. This real world data can serve as a reference toward high health care quality.

Detailed description

This is a prospective, observational, cohort study. Patients undergoing elective surgery will be invited to the study. The written informed consent will be obtained prior to participation. Demographic data, underlying condition, surgical procedures, consumption of anesthetics and analgesics, analgesic methods, postoperative complications, pain intensity and life quality will be collected from medical history and by questionnaires.

Conditions

Interventions

TypeNameDescription
OTHERERDS groupAfter anesthesia, extended-release dinalbuphine sebacate (ERDS) is injected into gluteus maximus with ultrasound guidance.

Timeline

Start date
2020-10-27
Primary completion
2022-09-30
Completion
2022-12-31
First posted
2020-10-08
Last updated
2025-09-25

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04578483. Inclusion in this directory is not an endorsement.