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Not yet recruitingNCT07900126Updated Oct 28, 2026

Clinical and Biological Parameters in Adolescent Idiopathic Scoliosis

An observational study in Adolescent Idiopathic Scoliosis (AIS), sponsored by Gaziler Physical Medicine and Rehabilitation Education and Research Hospital. Not yet recruiting. Open to participants aged 10 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-10-28.

Sponsored by Gaziler Physical Medicine and Rehabilitation Education and Research Hospital · Observational

Updated Oct 28, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
83
Ages
10 Years to 18 Years
Sex
All
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Study summary

This single-center, observational, cross-sectional study aims to investigate the association between fecal calprotectin levels and clinical characteristics in adolescents with idiopathic scoliosis. Clinical, radiological, anthropometric, nutritional, and laboratory parameters will be evaluated to explore potential relationships with curve severity.

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Conditions studied

  • Adolescent Idiopathic Scoliosis (AIS)

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Keywords

  • Spinal Deformity
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In context

Scoliosis

660 studies on the registry are indexed under Scoliosis; 186 are open to participants now.

This study's planned enrollment of 83 is close to the median of 84 across 256 observational studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital is the lead sponsor of 85 studies on the registry; 14 are open to participants now.

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

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Who can participate

Ages eligible
10 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adolescents aged 10-18 years diagnosed with idiopathic scoliosis who attend a specialized scoliosis outpatient clinic and meet the study eligibility criteria.

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

Adolescents aged 10-18 years with a confirmed diagnosis of idiopathic scoliosis (Cobb angle ≥10°).

No clinical evidence of acute or chronic infection or significant systemic inflammation.

No recent infection within the preceding three months.

No history of gastrointestinal disease or recent antibiotic/probiotic use.

No previous scoliosis surgery.

Voluntary participation with appropriate .

Exclusion criteria

Exclusion Criteria:

Congenital, neuromuscular, or syndromic scoliosis.

Inflammatory bowel disease, celiac disease, or other chronic inflammatory disorders, rheumatological disease, or .

Family history of inflammatory bowel disease or celiac disease.

Recent gastrointestinal symptoms, including diarrhea, gastrointestinal bleeding, unexplained abdominal pain, or weight loss.

Infection within the preceding three months.

Use of , NSAIDs, or medications within the preceding three months.

Pregnancy.

Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
83 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes
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What researchers measure

Primary outcomes

  1. Association Between Fecal Calprotectin Levels and Cobb Angle

    Fecal calprotectin levels (µg/g) will be measured and their association with radiographic Cobb angle (degrees) will be evaluated.

    Time frame: At enrollment (single assessment)

Secondary outcomes

  1. Scoliosis Progression Risk Index

    Association of fecal calprotectin levels with the Lonstein-Carlson progression risk index.

    Time frame: At enrollment (single assessment)

  2. Body Composition Parameters

    Association of fecal calprotectin levels with body mass index, fat mass, fat-free mass, and body fat percentage.

    Time frame: At enrollment (single assessment)

  3. Dietary Habits

    Association of fecal calprotectin levels with dietary habits assessed using a standardized questionnaire.

    Time frame: At enrollment (single assessment)

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No — Individual participant data will not be publicly shared due to participant privacy and confidentiality considerations.

No publications or documents are linked to this record.

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Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 28, 2026
Show all 1 update
  1. Oct 28, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07900126
Lead sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Collaborators
The Scientific and Technological Research Council of Turkey
Responsible party
Tuğba Atan, MD (Associate Professor of Physical Medicine and Rehabilitation, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital) — Principal investigator
First posted
Oct 28, 2026
Start date
Nov 1, 2026 (estimated)
Primary completion
May 1, 2027 (estimated)
Completion
Jun 1, 2027 (estimated)
Last update
Oct 28, 2026

Study contacts

Tuğba Atan, MD
Contact
tubaatan@gmail.com
+9 0 312 291 14 14

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 not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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