CI

At a glance

ClinicalIndex Comparison Record
N/AActive· 120 enrolled
Drug / intervention
Non-surgical +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04536909
NCT04536909N/AActive

Indication and Treatment of Adult Kyphoscoliosis

University of Bergen·observational·Posted Sep 3, 2020·Updated Sep 19, 2024

In Brief

An observational study evaluating Non-surgical and Surgical for Kyphoscoliosis. Active but no longer recruiting, targeting 120 participants across 5 sites in 3 countries.

Detailed Summary

Degeneration, iatrogenic-/idiopathic causes and fractures can lead to kypho- scoliotic deformities potentially resulting in pain and loss of function. The surgical strategies rely on surgeon preferences and type of deformity as well as clinical symptoms. The complication rate of surgical treatment is high. The aim of this study is to elucidate the indications for surgical treatment of kyphoscoliosis and evaluate the effectiveness of surgical and non-surgical outcome clinically and radiologically. The primary outcome for the PROMs and x-ray is at 12 months, but the investigators will also follow the patients with the PROMs and x-rays after 2,5 and 10 years.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsKyphoscoliosis
CountriesJapan, Norway, Sweden

Timeline

N/AActiveOverdue
2020202120222023202420252026
First PostedSep 3, 2020
Enrollment StartJan 1, 2020
Primary CompletionJan 1, 2024
Study CompletionJan 1, 2026
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 5.8 years ago

Interventions

Non-surgicalother

We have constructed a training program with help from physiotherapists from Rikshospitalet in Oslo, tailored for kyphotic- and scoliotic patients.

Surgicalprocedure

Surgery for correction of kyphotic- or scoliotic deformity.