CClinicalTrials.gg
Status unknownNCT02976571Updated May 9, 2018

Local and Intraperitoneal Analgetics in Gynecologic Laparoscopy for Post Operative Pain Relief

An interventional study of Bupivacaine in Postoperative Complications, sponsored by Wolfson Medical Center. Status unknown at 1 site in Israel. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-05-09.

Sponsored by Wolfson Medical Center · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified May 2018), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

A comparison between local and intraperitoneal analgetics to placebo, during laparoscopy, regarding post operative pain.

Read the detailed description

4 randomly assigned groups. Grop 1 will get sub cutaneous and intraperitoneal marcain. Grop 2 will get sub cutaneous marcaine and intraperitoneal saline. Grop 3 will get sub cutaneus saline and intraperitoneal marcaine. Grop 4 will get ub cutaneous and intraperitoneal saline

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Conditions studied

  • Postoperative Complications
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In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's planned enrollment of 120 is above the median of 75 across 4,344 interventional studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Wolfson Medical Center is the lead sponsor of 113 studies on the registry; 16 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 and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Elective laparoscopy

Exclusion criteria

Exclusion Criteria:

  • Laparotomy Vaginal operations Oncologic operations Chronic use of analgetics due to pelvic pain Pregnancy Operations lasts more than 3 hours
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Sub cutaneous+Intraperitoneal

    Sub cutaneous Bupivacaine+ Intraperitoneal bupivacaine

    Drug: Bupivacaine

  • Active comparator
    Sub cutaneous+Placebo

    Sub cutaneous Bupivacaine+ Intraperitoneal Nacl 0.9%

    Drug: Bupivacaine

  • Active comparator
    Placebo+Intraperitoneal

    Sub cutaneous Nacl 0.9%+ Intraperitoneal bupivacaine

    Drug: Bupivacaine

  • Placebo comparator
    Placebo+Placebo

    Sub cutaneous Nacl 0.9%+ Intraperitoneal Nacl 0.9%

    Drug: Bupivacaine

Interventions

  • DrugBupivacaine

    Sub cutaneous and/or Intraperitoneal Marcaine application

    Also known as: Marcaine

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What researchers measure

Primary outcomes

  1. Pain level during movement, 8 hours after laparoscopy

    Time frame: 8 hours

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Study locations

1 of 1 sites recruiting
  • Wolfson medical center
    H̱olon, Israel
    Recruiting
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References and documents

Publications

  • Gluck O, Barber E, Feldstein O, Tal O, Kerner R, Keidar R, Wolfson I, Ginath S, Bar J, Sagiv R. The effect of subcutaneous and intraperitoneal anesthesia on post laparoscopic pain: a randomized controlled trial. Sci Rep. 2021 Jan 8;11(1):81. doi: 10.1038/s41598-020-80130-6. PubMed 33420214 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 9, 2018, 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
NCT02976571
Lead sponsor
Wolfson Medical Center
Responsible party
Sponsor
First posted
Nov 29, 2016
Start date
Nov 2016
Primary completion
Dec 2018 (estimated)
Completion
Dec 2018 (estimated)
Last update
May 9, 2018

Study contacts

Ohad Gluck, MD
Contact
ohadgluck@gmail.com
97235028329
Elad Barer, MD
Contact
elad.barber@gmail.com
9725028329
Ohad Gluck, MD
principal investigator · Wolfson Medical Center

Oversight

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

Not currently enrolling

This study is status unknown, as verified in May 2018. You cannot join it, but the record below documents what was studied.

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