Researching the Useful of Barb Suture in Obese Patients Undergoing Posterior Cervical Surgery
Recruiting · NCT05895968 · Interventional (participants receive a specific treatment) · Lead sponsor: Xijing Hospital
View the official record on ClinicalTrials.gov →Interventions studied
posterior cervical surgery
What this trial is about
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.
Who can take part
Age range
28 Years to 85 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 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.
Exclusion criteria
- 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
- Skin injury or defect at the back of the neck
- Severe hypersensitivity
- Cold, fever, trauma or other infections in the week before surgery
- Infectious disease
- Psychosis could not cooperate with follow-up
Where it is running
1 location listed.
- Jia Yanyan - Xi'an, Shannxi Province, China