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CompletedNCT02782767Updated Feb 7, 2017

Comparison of Continuous Wound Catheter Infusion Versus Continuous Epidural Infusion in Abdominal Surgery

An interventional study of Wound catheter infusion and Epidural infusion in Upper Gastrointestinal Surgery, Post-operative Analgesia and Wound Infusion Catheter, sponsored by Post Graduate Institute of Medical Education and Research, Chandigarh. Completed at 1 site in India. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-02-07.

Sponsored by Post Graduate Institute of Medical Education and Research, Chandigarh · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

Comparison of efficacy in management of pain in abdominal surgery between epidural versus wound infusion catheter {catheter placed within the incision site}

02

Conditions studied

  • Upper Gastrointestinal Surgery
  • Post-operative Analgesia
  • Wound Infusion Catheter
  • Upper Midline Incision

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03

In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's enrollment of 40 is below the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

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Lead sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh is the lead sponsor of 290 studies on the registry; 42 are open to participants now.

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

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Who can participate

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

Inclusion criteria

  • ASA PS I-III , undergoing upper gastrointestinal surgery involving upper midline incision

Exclusion criteria

Exclusion Criteria:

  • Refusal to give consent.
  • Contraindication to epidural analgesia (e.g.localized sepsis , Raised ICP , Myelopathy , Peripheral neuropathy ,Inherited coagulopathy)
  • Addiction to opioids, or alcohol, or history of any other substance abuse.
  • Allergy to local anaesthetic drugs.
  • Pregnancy.
  • Inability to communicate (e.g. known psychiatric disorders)
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
40 participants (actual)

Study arms

  • Active comparator
    Epidural catheter infusion

    epidural catheter in the thoracic vertebra level to provide local anesthetic infusion

    Other: Epidural infusion

  • Experimental
    Wound catheter infusion

    A multiorificed wound infusion catheter kept within the incision site to provide continuous local anesthetic infusion

    Other: Wound catheter infusion

Interventions

  • OtherWound catheter infusion

    Wound catheter has multiple holes spread around 360 degrees throughout its active length. It is placed in the musculofascial plane during closure of the wound. Local anaesthetic infusion will be delivered through the catheter.

  • OtherEpidural infusion

    Epidural catheter will be placed in the level T7-T9 , and local anaesthetic infusion will be given

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What researchers measure

Primary outcomes

  1. NRS (Numerical Rating Score) in the two groups postoperatively

    Time frame: 24 hrs post surgery

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Study locations

1 site
  • PGIMER
    Chandigarh, 160012, India
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 7, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02782767
Lead sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Responsible party
Arun Raja T (Junior Resident, Post Graduate Institute of Medical Education and Research, Chandigarh) — Principal investigator
First posted
May 25, 2016
Start date
May 2016
Primary completion
Jan 2017
Completion
Jan 2017
Last update
Feb 7, 2017

Study contacts

Arun Raja Thangavel, MBBS
principal investigator · Junior Resident , MD Anaesthesia and Intensive care

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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