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CompletedNCT07625397IMRAN-LPUpdated Jun 4, 2026

Imran Technique for Spinal Anesthesia and Lumbar Puncture

An interventional study of Conventional Sitting Position and Imran Technique in Spinal Anesthesia, Lumbar Puncture and Patient Positioning, sponsored by Wah Medical college , POF hospital. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-06-04.

Sponsored by Wah Medical college , POF hospital · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Non-randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This quasi-experimental prospective clinical trial was conducted to compare the conventional sitting position with the Imran Technique, a novel ergonomic patient-positioning method, for spinal anesthesia and lumbar puncture. A total of 200 adult participants requiring spinal anesthesia for surgical procedures or diagnostic lumbar puncture were allocated into two groups. The study aimed to evaluate procedural success, procedural efficiency, patient comfort, operator ergonomics, and procedure-related complications associated with the two positioning techniques.

Read the detailed description

This quasi-experimental prospective clinical trial was designed to compare the conventional sitting position and the Imran Technique during spinal anesthesia and lumbar puncture procedures. Adult participants aged 18 to 65 years who required spinal anesthesia for surgical procedures or diagnostic lumbar puncture were enrolled and allocated into two groups.

Participants in the control group underwent the procedure using the conventional sitting position, while participants in the intervention group underwent the procedure using the Imran Technique. The primary outcome measure was first-attempt procedural success. Secondary outcome measures included total procedural time, positioning-to-needle insertion time, number of needle attempts, needle redirections, intervertebral space changes, overall procedural success, need for operator assistance, patient comfort, ability to maintain position, operator strain, accessibility of the intervertebral space, and procedure-related complications.

The study was conducted at the Intensive Care Unit of the Department of Anaesthesiology, POF Hospital, Wah Cantt, Pakistan, following Institutional Review Board approval and written informed consent procedures.

02

Conditions studied

  • Spinal Anesthesia
  • Lumbar Puncture
  • Patient Positioning

Keywords

  • Imran Technique
  • Spinal Anesthesia
  • Lumbar Puncture
  • Patient Positioning
  • Ergonomics
  • Procedural Success
  • Anesthesia Technique
03

In context

Lead sponsor

Wah Medical college , POF hospital is the lead sponsor of 4 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult participants aged 18 to 65 years
  • Participants requiring spinal anesthesia for surgical procedures or diagnostic lumbar puncture
  • Participants medically suitable for spinal anesthesia or lumbar puncture
  • Participants able to assume and maintain the assigned procedural position
  • Participants who provided written informed consent

Exclusion criteria

Exclusion Criteria:

  • Age below 18 years or above 65 years
  • Previous spinal surgery
  • Significant spinal deformity
  • Local infection at the puncture site
  • Coagulopathy or bleeding disorders
  • Raised intracranial pressure
  • Severe hemodynamic instability
  • Inability to maintain the assigned procedural position
  • Refusal to participate or inability to provide informed consent
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (actual)

Study arms

  • Active comparator
    Conventional Sitting Position

    Participants underwent spinal anesthesia or lumbar puncture using the conventional sitting position according to standard institutional practice.

    Procedure: Conventional Sitting Position

  • Experimental
    Imran Technique

    Participants underwent spinal anesthesia or lumbar puncture using the Imran Technique, a novel ergonomic positioning method designed to improve lumbar flexion, operator ergonomics, and procedural access.

    Procedure: Imran Technique

Interventions

  • ProcedureConventional Sitting Position

    Standard sitting patient positioning used for spinal anesthesia and lumbar puncture procedures.

  • ProcedureImran Technique

    A novel ergonomic patient positioning technique for spinal anesthesia and lumbar puncture involving lateral operator positioning and assisted lumbar flexion to improve procedural access and success.

06

What researchers measure

Primary outcomes

  1. First Attempt Procedural Success

    Successful spinal anesthesia or lumbar puncture achieved with a single skin puncture on the first attempt.

    Time frame: During the procedure (up to 30 minutes)

Secondary outcomes

  1. Total Procedural Time

    Total time required from patient positioning to successful completion of spinal anesthesia or lumbar puncture.

    Time frame: During the procedure (up to 30 minutes)

  2. Number of Needle Attempts

    Total number of skin puncture attempts required to successfully complete the procedure.

    Time frame: During the procedure

  3. Needle Redirections

    Number of needle redirections required during spinal anesthesia or lumbar puncture.

    Time frame: During the procedure

  4. Intervertebral Space Changes

    Number of intervertebral space changes required to successfully complete the procedure.

    Time frame: During the procedure

  5. Overall Procedural Success

    Successful completion of spinal anesthesia or lumbar puncture regardless of the number of attempts required.

    Time frame: During the procedure (up to 30 minutes)

  6. Patient Comfort Assessed Using a 0-10 Numeric Rating Scale (NRS)

    Participant comfort during positioning and spinal anesthesia/lumbar puncture was assessed using a 0-10 Numeric Rating Scale, where lower scores indicate greater comfort.

    Time frame: During the procedure

  7. Ability to Maintain Position Assessed Using an Investigator-Defined 3-Category Scale

    Participant ability to maintain the assigned procedural position was assessed using an investigator-defined 3-category scale: Easy, Moderate, or Difficult.

    Time frame: During the procedure

  8. Operator Strain Assessed Using an Investigator-Defined 4-Category Ergonomic Scale

    Operator physical strain during the procedure was assessed using an investigator-defined 4-category scale: None, Mild, Moderate, or Severe.

    Time frame: During the procedure

  9. Accessibility of Intervertebral Space Assessed Using an Investigator-Defined 3-Category Operator Rating Scale

    Accessibility of the intervertebral space was assessed by the operator using an investigator-defined 3-category scale: Easy, Acceptable, or Difficult.

    Time frame: During the procedure

  10. Procedure-Related Complications

    Occurrence of procedure-related events including paresthesia, bloody tap, hypotension, bradycardia, or procedural failure.

    Time frame: uring the procedure and immediately after procedure (up to 1 hour)

07

Study locations

1 site
  • Wah Medical College, POF Hospital Wah cantt
    Wah, Punjab Province 4070, Pakistan
08

References and documents

Individual participant data

Plan to share: Yes — Individual participant data that underlie the results reported in the published article, after de-identification.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07625397
Lead sponsor
Wah Medical college , POF hospital
Responsible party
Sponsor
First posted
Jun 4, 2026
Start date
Mar 2, 2026
Primary completion
Mar 31, 2026
Completion
Mar 31, 2026
Last update
Jun 4, 2026

Study contacts

Imran Ul Haq, MBBS, FCPS
principal investigator · Wah Medical College (NUMS) / POF Hospital Wah Cantt, Pakistan

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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