Researching the Useful of Barb Suture in Obese Patients Undergoing Posterior Cervical Surgery

Air Force Military Medical University of People's Liberation Army

Status: Enrolling

Conditions: Barbed Suture; Cervical Spinal Stenosis; Posterior Cervical Spine Surgery

Treatments: Procedure: posterior cervical surgery

Study type: Interventional

Funder types: Other

Identifiers

NCT05895968

KY20232136-F-1

Details and patient eligibility

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.

Enrollment: 60 estimated patients

Sex: All

Ages: 28 to 85 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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60 participants in 4 patient groups

Preoperative

No Intervention group

postoperative (2 weeks)

Experimental group

Treatment:

Procedure: posterior cervical surgery

postoperative (4 weeks)

Experimental group

Treatment:

Procedure: posterior cervical surgery

postoperative (3 months)

Experimental group

Treatment:

Procedure: posterior cervical surgery