ClinicalTrials.gg
CompletedNCT05752838Updated Mar 3, 2023

A Questionnaire Survey Study for Exploring Outcomes for Patients With Disc Herniation

An observational study in Lumbar Disc Herniation, sponsored by Jaseng Medical Foundation. Completed at 1 site in South Korea. Open to participants aged 19 Years to 69 Years. Per ClinicalTrials.gov, last updated 2023-03-03.

Sponsored by Jaseng Medical Foundation · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
500
Ages
19 Years to 69 Years
Sex
All
01

Study summary

Background: The selection of primary outcomes that reflect the real symptoms and conditions of patients is instrumental in clinical studies on the effectiveness of specific treatment modalities. This study aimed to explore the appropriate outcomes that reflect the real-world needs and concerns of patients with lumbar disc herniation (LDH) and provide a basis for designing related clinical trials.

Methods and Findings: This cross-sectional nationwide web-based survey study was conducted in South Korea in November 2022. Patients who were diagnosed with LDH and had LDH-related radiating leg pain were enrolled. The questionnaire consisted of 5 parts: basic characteristics, disease onset, symptom and severity, priority symptoms for improvement, and important factors in treatment. Overall, 500 patients (100 patients from the each age group) were enrolled.

02

Conditions studied

  • Lumbar Disc Herniation
03

In context

Intervertebral Disc Displacement

489 studies on the registry are indexed under Intervertebral Disc Displacement; 104 are open to participants now.

This study's enrollment of 500 is above the median of 100 across 123 observational studies indexed under Intervertebral Disc Displacement.

Browse Intervertebral Disc Displacement studies →

Lead sponsor

Jaseng Medical Foundation is the lead sponsor of 68 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 69 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

All 19-69 patients who were diagnosed with LDH and had LDH-related radiating leg in Korea

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • diagnosed of LDH
  • age 19-69 years
  • presence of LDH-related symptoms such as pain, numbness, weakness, or tingling in the legs
  • agree to informed consent form

Exclusion criteria

Exclusion Criteria:

  • severe mental illness and intellectual disabilities that prevented independence in answering the questionnaire
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
500 participants (actual)
Patient registry
No

Groups and cohorts

  • Diagnosed with LDH and had LDH-related radiating leg pain

    Other: No intervention

Interventions

  • OtherNo intervention

    This is a survey study, and there were no intervention

06

What researchers measure

Primary outcomes

  1. survey basic characteristics

    Time frame: 1 day

  2. disease onset survey

    Time frame: 1 day

  3. symptom and its severity survey

    Time frame: 1 day

  4. priority symptoms for improvement survey

    Time frame: 1 day

  5. important factors in treatment survey

    Time frame: 1 day

07

Study locations

1 site
  • Jaseng Medical Foundation
    Seoul, Gangnam-gu 06110, South Korea
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Nov 2022 to primary completion in Nov 2022, 0 months.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 22, 2023
First posted
Mar 3, 2023
StartActual
Nov 15, 2022
Primary completionActual
Nov 16, 2022
CompletionActual
Nov 16, 2022
Last update
Mar 3, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 3, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05752838
Lead sponsor
Jaseng Medical Foundation
Responsible party
Sponsor
First posted
Mar 3, 2023
Start date
Nov 15, 2022
Primary completion
Nov 16, 2022
Completion
Nov 16, 2022
Last update
Mar 3, 2023

Study contacts

In-Hyuk Ha, PhD
principal investigator · Jaseng Medical Foundation

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion