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Imran Technique for Spinal Anesthesia and Lumbar Puncture

Imran's Approach: A Quasi-Experimental Prospective Comparative Study of an Alternative Positioning Technique for Spinal Anesthesia and Lumbar Puncture

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07625397
Acronym
IMRAN-LP
Enrollment
200
Registered
2026-06-04
Start date
2026-03-02
Completion date
2026-03-31
Last updated
2026-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Puncture, Patient Positioning, Spinal Anesthesia

Keywords

Imran Technique, Spinal Anesthesia, Lumbar Puncture, Patient Positioning, Ergonomics, Procedural Success, Anesthesia Technique

Brief 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.

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.

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.

Sponsors

Wah Medical college , POF hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

Participants were allocated into two parallel groups to compare the conventional sitting position with the Imran Technique for spinal anesthesia and lumbar puncture.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
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

* 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

Design outcomes

Primary

MeasureTime frameDescription
First Attempt Procedural SuccessDuring the procedure (up to 30 minutes)Successful spinal anesthesia or lumbar puncture achieved with a single skin puncture on the first attempt.

Secondary

MeasureTime frameDescription
Total Procedural TimeDuring the procedure (up to 30 minutes)Total time required from patient positioning to successful completion of spinal anesthesia or lumbar puncture.
Number of Needle AttemptsDuring the procedureTotal number of skin puncture attempts required to successfully complete the procedure.
Needle RedirectionsDuring the procedureNumber of needle redirections required during spinal anesthesia or lumbar puncture.
Intervertebral Space ChangesDuring the procedureNumber of intervertebral space changes required to successfully complete the procedure.
Overall Procedural SuccessDuring the procedure (up to 30 minutes)Successful completion of spinal anesthesia or lumbar puncture regardless of the number of attempts required.
Patient Comfort Assessed Using a 0-10 Numeric Rating Scale (NRS)During the procedureParticipant comfort during positioning and spinal anesthesia/lumbar puncture was assessed using a 0-10 Numeric Rating Scale, where lower scores indicate greater comfort.
Ability to Maintain Position Assessed Using an Investigator-Defined 3-Category ScaleDuring the procedureParticipant ability to maintain the assigned procedural position was assessed using an investigator-defined 3-category scale: Easy, Moderate, or Difficult.
Operator Strain Assessed Using an Investigator-Defined 4-Category Ergonomic ScaleDuring the procedureOperator physical strain during the procedure was assessed using an investigator-defined 4-category scale: None, Mild, Moderate, or Severe.
Accessibility of Intervertebral Space Assessed Using an Investigator-Defined 3-Category Operator Rating ScaleDuring the procedureAccessibility of the intervertebral space was assessed by the operator using an investigator-defined 3-category scale: Easy, Acceptable, or Difficult.
Procedure-Related Complicationsuring the procedure and immediately after procedure (up to 1 hour)Occurrence of procedure-related events including paresthesia, bloody tap, hypotension, bradycardia, or procedural failure.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORImran Ul Haq, MBBS, FCPS

Wah Medical College (NUMS) / POF Hospital Wah Cantt, Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 5, 2026