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Spinal StenosisERAS in SpineNCT06577389

Enhanced Recovery After Surgery for Spine Fusion Surgeries in the Elderly

An observational study of Spinal Stenosis, run by Sixth Affiliated Hospital of Xinjiang Medical University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

elderly patients in our hospital who received spinal fusion surgery after the year 2025 will receive ERAS treatment. Read more about this study

Who is it for?
Ages 60 years and older
Conditions the study is for
Spinal Stenosis
What is being tested?
Enhanced recovery after surgery
How many people
1,500 participants
Where
No sites listed yet
Study dates
1 Jan 2025to 31 Dec 2028
How long will I take part?
12 Months
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: elderly patients who received spinal fusion surgeries

Who may be able to join

  • elderly patients who received spinal fusion surgeries

Who cannot join

  • patients who received non-fusion surgeries

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Aikeremujiang Professor Ai contact

+8618810914750

muheremua@bjmu.edu.cn

About this study

elderly patients in our hospital who received spinal fusion surgery after the year 2025 will receive ERAS treatment.

Conditions
Spinal Stenosis
Being tested
Enhanced recovery after surgery
Keywords
spine fusion surgery
Medical subject headings
Spinal Stenosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Enhanced recovery after surgeryOther

    The ERAS program for lumbar fusion surgery will be implemented.

Study groups in NCT06577389
Study groupRoleWhat they receive
elderly after spine fusion surgerypatients receive Enhanced recovery after spinal fusion surgery
Receives: Other: Enhanced recovery after surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. ambulation time

    Measured: 7 days

Secondary outcomes (2)
  1. mean hospital length of stay

    Measured: one month

  2. cost of hosptial stay

    Measured: 1 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Aug 2024
  2. Study start1 Jan 2025 (estimated)
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,500 participants (estimated)
Target duration
12 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06577389
Sponsor's protocol ID
SixthAHXinjiang
Acronym
ERAS in Spine
Status last verified
Aug 2024
First submitted
27 Aug 2024
Last updated
29 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: will decide before the year 2026

Questions about this trial

What is this clinical trial studying?

An observational study of Spinal Stenosis, run by Sixth Affiliated Hospital of Xinjiang Medical University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 29 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Aikeremujiang Professor Ai (+8618810914750, muheremua@bjmu.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

ambulation time (time frame: 7 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2024.

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