Disc HerniationNCT06141551
Intradural Disc Herniation: a Case Report and Review of Complications
An observational study of Disc Herniation, run by Gansu Provincial Hospital at 1 site in China.
Trial 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… Read more about this study
- Who is it for?
- Ages 40 to 40 years, men only
- Conditions the study is for
- Disc Herniation
- What is being tested?
- total laminectomy decompression
- Type of treatment
- Surgery or procedure
- How many people
- 1 participants
- Where
- 1 siteChina
- Study dates
- 1 Oct 2023to 3 Dec 2023
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 40 years
- Men only
- No healthy volunteers
- Adult
Study population: A male 40-year-old patient with IDH
Who may be able to join
- IDH patients
Who cannot join
- no
Trial locations and contacts
1 site in 1 country.
About this study
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.
Read the detailed description
We collect the patient's personal history, family history, reason for visit, visit flow, clinical data, pathology reports, and surgical images and videos.
- Conditions
- Disc Herniation
- Being tested
- total laminectomy decompression
- Keywords
- Intradural disc herniation, Complications, Degenerative spinal disease, Decompression
- Medical subject headings
- Intervertebral Disc Displacement
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
total laminectomy decompressionProcedure or surgery
Also called posterior approach lumbar spinal fusion
Surgical decompression
What is being measured
The primary outcome is the main question the study is designed to answer.
physiology
Grayish-white tissue identified as degenerated disc tissue was removed from the patient's lumbar spine partially within the dura mater
Measured: 07/2023
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Nov 2023
- Study start1 Oct 2023
- Primary completion2 Dec 2023 (estimated)
- Study completion3 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Disc HerniationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Retrospective
- Enrolment
- 1 participants (actual)
Sponsor and investigators
- Lead sponsor
- Gansu Provincial Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, ZhenHu, Gansu Provincial Hospital
- Investigators
- Hui Zhang, Dr, Study director, Gansu Provincial People's Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06141551
- Sponsor's protocol ID
- CR20231001
- Status last verified
- Nov 2023
- First submitted
- 15 Nov 2023
- Last updated
- 21 Nov 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The patients in this study rejected this
Study at a glance
From the registry record, last updated by the sponsor on 21 Nov 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Intradural Disc Herniation: a Case Report and Review of Complications
- ClinicalTrials.gov ID
- NCT06141551
- Acronym / sponsor ID
- CR20231001
- Conditions
- Disc Herniation
- Keywords
- Intradural disc herniation, Complications, Degenerative spinal disease, Decompression
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Gansu Provincial HospitalUniversity, hospital or other
- Study start
- 1 Oct 2023 (actual)
- Primary completion
- 2 Dec 2023 (estimated)
- Study completion
- 3 Dec 2023 (estimated)
- First posted
- 21 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
We collect the patient's personal history, family history, reason for visit, visit flow, clinical data, pathology reports, and surgical images and videos.
Study design
- Observational model
- Case only
- Time perspective
- Retrospective
Who may qualify
- Ages
- 40 to 40 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- A male 40-year-old patient with IDH
Key inclusion criteria (1 listed)
- IDH patients
Key exclusion criteria (1 listed)
- no
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| total laminectomy decompressionAlso: posterior approach lumbar spinal fusionSurgical decompression | Procedure or surgery | – |
Primary outcome
physiology
Time frame: 07/2023
Grayish-white tissue identified as degenerated disc tissue was removed from the patient's lumbar spine partially within the dura mater
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Nov 2023.
- Individual participant dataSharing planned: No. The patients in this study rejected this
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Hui Zhang, Dr study director
Gansu Provincial People's Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Disc Herniation, run by Gansu Provincial Hospital at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 21 Nov 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
physiology (time frame: 07/2023). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Nov 2023; AzTrials last refreshed its copy on 8 Nov 2026.