NCT05895968Recruiting
Researching the Useful of Barb Suture in Obese Patients Undergoing Posterior Cervical Surgery
A Controlled Clinical Study on the Safety and Effectiveness of Barb Suture in Obese Patients Undergoing Posterior Cervical Surgery
Source: ClinicalTrials.gov · Last updated 30 Jul 2026
Brief summary (registry, in English)
Through a single-center, exploratory clinical study, the safety and effectiveness of using barb wire in the incision and suture of posterior cervical surgery in obese patients were evaluated, providing a basis for its wide clinical application in posterior cervical surgery.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 25 May 2023
- Start date
- 1 Jan 2023
- Primary completion date
- 31 Jan 2023
- Lead sponsor
- Xijing Hospital
- Diseases
- Obesity
- NCT number
- NCT05895968
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 1 Jan 2023 to the primary completion date, 31 Jan 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Cold, fever, trauma or other infections in the week before surgery
Other illness
- A history of wasting diseases associated with malignancy and chemoradiotherapy that may interfere with wound healing
- History of dermatosis
- History of immune system diseases
- History of blood diseases
- Severe hypersensitivity
- Infectious disease
Other
- Skin injury or defect at the back of the neck
- Psychosis could not cooperate with follow-up
Who the study is looking for
- Symptoms and signs of the patients were typical. MRI showed single or multiple central herniation of C3-C7 intervertebral discs or spinal stenosis at corresponding levels, which confirmed cervical myeloid cervical spondylosis or cervical spinal stenosis.
- Preoperative routine tests and examinations showed no contraindications.
- BMI≥28
- Informed consent was obtained from the patient and his family, informed consent was signed, and a complete follow-up was completed after surgery.
Age in the registry: 28 years to 85 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Jia Yanyan Coordinator of this site? Confirm its status | Xi'an | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.