NCT06141551

Brief Summary

This observational study collects clinical data as well as pathological reports from a patient with an intradural disc herniation, reports on the course of the patient's recovery through surgical treatment, summarizes the complications of this type of disease, and provides new ideas for improving the chances of preoperative diagnosis.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Oct 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2023

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 15, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 21, 2023

Completed
11 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 2, 2023

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 3, 2023

Completed
Last Updated

November 21, 2023

Status Verified

November 1, 2023

Enrollment Period

2 months

First QC Date

November 15, 2023

Last Update Submit

November 15, 2023

Conditions

Disc Herniation

Keywords

Intradural disc herniationComplicationsDegenerative spinal diseaseDecompression

Outcome Measures

Primary Outcomes (1)

  • physiology

    Grayish-white tissue identified as degenerated disc tissue was removed from the patient's lumbar spine partially within the dura mater

    07/2023

Interventions

total laminectomy decompressionPROCEDURE

Surgical decompression

Also known as: posterior approach lumbar spinal fusion

Eligibility Criteria

Age40 Years - 40 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

A male 40-year-old patient with IDH

You may qualify if:

  • IDH patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gansu Provincial People's Hospital

Lanzhou, Gansu, 730000, China

Location

MeSH Terms

Conditions

Intervertebral Disc Displacement

Condition Hierarchy (Ancestors)

Spinal DiseasesBone DiseasesMusculoskeletal DiseasesHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Officials

  • Hui Zhang, Dr

    Gansu Provincial People's Hospital

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
doctor-in-charge

Study Record Dates

First Submitted

November 15, 2023

First Posted

November 21, 2023

Study Start

October 1, 2023

Primary Completion

December 2, 2023

Study Completion

December 3, 2023

Last Updated

November 21, 2023

Record last verified: 2023-11

Data Sharing

IPD Sharing
Will not share

The patients in this study rejected this

Locations

CN(1)