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The Application of Enhanced Recovery After Surgery Clinical Pathway in Posterior Cervical Spine Surgery

China400 participantsStarted 2020-08-01

Plain-language summary

This study intends to establish a multidisciplinary collaborative ERAS clinical pathway of cervical posterior surgery,and to verify its effectiveness, safety and value in health economics.

Who can participate

Age range18 Years – 70 Years

SexALL

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Inclusion criteria

✓. Age 18-70, gender unlimited;
✓. Diagnostic diagnosis of cervical spondylosis and consistent with the indications of posterior spinal canal extended laminoplasty;
✓. Basis of serious diseases of centerlessness, brain, lung, kidney or other important organs, preoperative ASA score I-II;
✓. Agree to participate in the study and sign the informed consent.

What they're measuring

range of motion on X - ray

Timeframe: preoperation

range of motion on X - ray

Timeframe: intraoperation

range of motion on X - ray

Timeframe: 72 hours after surgery

range of motion on X - ray

Timeframe: 3 months after surgery

range of motion on X - ray

Timeframe: 6 months after surgery

Japanese Orthopaedic Association Cervical Myelopathy Evaluation Questionnaire（JOACMEQ）

Timeframe: preoperation

Japanese Orthopaedic Association Cervical Myelopathy Evaluation Questionnaire（JOACMEQ）

Timeframe: intraoperation

Japanese Orthopaedic Association Cervical Myelopathy Evaluation Questionnaire（JOACMEQ）

Timeframe: 72 hours after surgery

Trial details

NCT IDNCT05149404

SponsorPeking University Third Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-12-30

Contact for this trial

Yu Sun, Dr.

13501221484 sunyuor@vip.sina.com

View on ClinicalTrials.gov More Cervical Spondylotic Myelopathy trials