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A Randomized Controlled Study on the Treatment of Sacral Canal Cysts With Sacral Canal Reinforcement (ARCSTSCC)

P

Peking University

Status

Unknown

Conditions

Tarlov Cysts

Treatments

Procedure: plasty treatment
Procedure: entraped treatment

Study type

Interventional

Funder types

Other

Identifiers

NCT04465305
PekingUTHNSD

Details and patient eligibility

About

The subject will treat 68 patients with symptomatic sacral canal cysts as the research object, and adopt a randomized controlled research method, respectively, using two methods of reinforcement and reconstruction of the nerve root sleeve, sacroplasty and nerve root sleeve plasty, and observed the operation of the patient Complications, preoperative and postoperative short-term and long-term VAS pain scores, JOA neural function scores, and changes in cyst size on imaging examinations, to evaluate the safety of nerve root sleeve reconstruction and sacroplasty in reducing the safety of postoperative cyst recurrence Sex and effectiveness, so as to further improve the surgical treatment of sacral canal cysts, improve the curative effect, and formulate the operation specifications for the treatment of sacral canal cyst

Full description

In this subject, a cohort observation method was used to observe 52 patients with two types of surgical removal of hematoma in the basal ganglia under the guidance of frontal ultrasound through keyhole neuroendoscopy and microsurgery for hematoma removal under the guidance of frontal ultrasound. They were divided into endoscopic surgery group and microsurgery. In the endoscopic surgery group, 26 cases were treated with keyhole neuroendoscopy under the guidance of frontal ultrasound for hematoma removal in the basal ganglia area, and 26 cases in the microsurgery group were treated by craniotomy microsurgery hematoma removal surgery. Observe the removal rate of surgical hematoma in the two groups And the safety of the operation and the GCS score, GOS score and MRI examination of nerve fiber damage and postoperative complications at 1 week, 1 month, and 3 months after the operation. Observe and analyze the improvement of the hematoma clearance rate in the endoscopic surgery group. And whether it has an advantage in terms of efficacy

Enrollment

68 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Symptomatic nerve root cysts diagnosed by MRI
  2. Intact cyst capsule, no defect of sacral canal lamina
  3. No other diseases of nervous system, pelvic floor and important organs
  4. Agree inclusion

Exclusion criteria

a ) Non-radiculent cysts or asymptomatic cysts b) Cysts cause severe bone erosion to lamina resorption c) Combined with other diseases of nervous system, pelvic floor and important organs d) Disagree to join e) Cannot complete follow-up -

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

68 participants in 2 patient groups

enraped group
Experimental group
Description:
patients with a new treatment of tarlov cysts
Treatment:
Procedure: entraped treatment
Procedure: plasty treatment
plasty group
Active Comparator group
Description:
patients with traditional treatment of tarlov cysts
Treatment:
Procedure: plasty treatment

Trial contacts and locations

1

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Central trial contact

wu chao; liu bin

Data sourced from clinicaltrials.gov

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