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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-01

Study Completion Date

2025-12-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Cervical Spinal Stenosis Posterior Cervical Spine Surgery Barbed Suture

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Preoperative

Group Type NO_INTERVENTION

No interventions assigned to this group

postoperative (2 weeks)

Group Type EXPERIMENTAL

posterior cervical surgery

Intervention Type PROCEDURE

The patients were operated by the posterior cervical surgery, which were used with the barbed to suture the deep fascia.

postoperative (4 weeks)

Group Type EXPERIMENTAL

posterior cervical surgery

Intervention Type PROCEDURE

The patients were operated by the posterior cervical surgery, which were used with the barbed to suture the deep fascia.

postoperative (3 months)

Group Type EXPERIMENTAL

posterior cervical surgery

Intervention Type PROCEDURE

The patients were operated by the posterior cervical surgery, which were used with the barbed to suture the deep fascia.

Interventions

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posterior cervical surgery

The patients were operated by the posterior cervical surgery, which were used with the barbed to suture the deep fascia.

Intervention Type PROCEDURE

Eligibility Criteria

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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

Minimum Eligible Age

28 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No