Fetal Alcohol Syndrome (FAS) Clinical Trials

Find Fetal Alcohol Syndrome (FAS) Clinical Trials Near You

Quality of Life, Psychosocial Burden, and Structural-functional Status in Adults With Spinal Deformity.

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study examines which factors influence quality of life in adults with a spinal deformity. It looks at imaging findings together with pain, daily functioning, psychosocial factors, and frailty to support more person-centred care. A total of 320 adults will participate in three groups: conservative treatment, first corrective surgery, or reoperation. All care follows standard practice; no experimental treatments are added. Participants complete questionnaires, and routine FASD tests and existing EOS/X-ray images may be used. Follow-up lasts up to 2 years, with scheduled assessments depending on whether treatment is surgical or conservative.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures

• Age at inclusion 18 years or older.

• Diagnosed with Adult spinal deformity

• Planned routine management through one of the following pathways:

‣ Conservative/non-operative management;

⁃ Primary ASD surgery;

⁃ Revision ASD surgery.

• Ability to complete the Dutch-language questionnaire package.

Locations
Other Locations
Belgium
UZ Leuven
RECRUITING
Leuven
Contact Information
Primary
Lieven Moke, prof. dr.
lieven.moke@uzleuven.be
016338827
Time Frame
Start Date: 2026-08
Estimated Completion Date: 2029-07
Participants
Target number of participants: 320
Treatments
Experimental: Fist corrective surgery
patients undergoing a first corrective surgery
Experimental: Reoperation
patients undergoing a reoperation
No_intervention: treated conservatively
patients who are treated conservatively
Related Therapeutic Areas
Sponsors
Leads: Universitaire Ziekenhuizen KU Leuven

This content was sourced from clinicaltrials.gov