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NCT01535001COMPLETEDanonymous

Structured Non-operative Treatment of Knee Osteoarthritis - a Randomized Controlled Trial of Pain, Physical Function and Quality of Life With 12months Follow-up

Sponsor

Source record

Northern Orthopaedic Division, Denmark

Phase

Source record

NA

Modality

AI-normalized

behavioral intervention

Target

AI-normalized

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Indication / condition

AI-normalized

Osteoarthritis of the Knee

Intervention

Source record

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Source & freshness

Source record

NCT ID

NCT01535001

Original source

ClinicalTrials.gov

Source last updated

Oct 16, 2017

Ingested at

Jun 09, 2026

Internal sync

Jun 09, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT01535001

Title

Structured Non-operative Treatment of Knee Osteoarthritis - a Randomized Controlled Trial of Pain, Physical Function and Quality of Life With 12months Follow-up

Sponsor

Northern Orthopaedic Division, Denmark

Status

COMPLETED

Phase

NA

Condition raw

Osteoarthritis of the Knee

Condition normalized

Osteoarthritis of the Knee

Modality raw

behavioral intervention

Modality normalized

behavioral intervention

Target raw

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Target normalized

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Interventions

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Public preview

Source record

The purpose of this study is to test whether an algorithm for systematic non-surgical treatment consisting of corrective insoles, neuromuscular training, weight loss, patient education and pharmacological treatment with paracetamol, non steroidal anti inflammatory drugs (NSAIDs) and Pantoprazole provides further improvement in pain, function and quality of life than standard non-surgical treatment (information on the disease and how to treat it) in patients with knee osteoarthritis.

The H1-hypothesis is that the treatment algorithm results in a greater increase in quality of life and functional capacity and greater reduction in pain than standard treatment at the primary endpoint, which is follow-up 12months after the start of the treatment.

See statistical analysis plan available under "Links" for further description of the study.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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TrialSignal

Clinical trial intelligence report

Structured Non-operative Treatment of Knee Osteoarthritis - a Randomized Controlled Trial of Pain, Physical Function and Quality of Life With 12months Follow-up

Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.

Generated

Jun 13, 2026

NCT ID

NCT01535001

Status

COMPLETED

Phase

NA

Sponsor

Northern Orthopaedic Division, Denmark

Executive brief

Investment-Ready Snapshot

The purpose of this study is to test whether an algorithm for systematic non-surgical treatment consisting of corrective insoles, neuromuscular training, weight loss, patient education and pharmacological treatment with paracetamol, non steroidal anti inflammatory drugs (NSAIDs) and Pantoprazole provides further improvement in pain, function and quality of life than standard non-surgical treatment (information on the disease and how to treat it) in patients with knee osteoarthritis. The H1-hypothesis is that the treatment algorithm results in a greater increase in quality of life and functional capacity and greater reduction in pain than standard treatment at the primary endpoint, which is follow-up 12months after the start of the treatment. See statistical analysis plan available under "Links" for further description of the study.

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedOct 16, 2017
Internal syncJun 09, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT01535001

Indication

Osteoarthritis of the Knee

Modality

behavioral intervention

Target

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Intervention

Neuromuscular training (NEMEX-TJR), Information, Paracetamol, Burana, Pantoprazole, Dietary counseling, Patient education, Insoles

Source record

Protocol Description

Detailed source ingestion pending.

Source record

Outcome Measures

Detailed source ingestion pending.

Source record

Eligibility

Detailed source ingestion pending.

AI analysis

Known Results And Readout Context

Detailed source ingestion pending.

IP intelligence

Patent And IP Landscape

Detailed source ingestion pending.

Source record

Contacts

Detailed source ingestion pending.