CClinicalTrials.gg
Status unknownNCT02826876Updated Jul 11, 2016

The Efficacy of Surgical Site Treatment With Ropivacaine in Laparoscopic Surgery

An interventional study of Topical use and laparoscopic repair of inguinal hernia in Pain, sponsored by Western Galilee Hospital-Nahariya. Status unknown at 1 site in Israel. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2016-07-11.

Sponsored by Western Galilee Hospital-Nahariya · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2016), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Using local analgesia in laparoscopic surgery in order to reduce pain and to reduce the use of narcotic drugs.

Read the detailed description

At the end of laparoscopic surgery the investigators will spray ropivacaine in the surgical site; and later the investigators will monitor pain intensity and use of analgesic drugs

02

Conditions studied

  • Pain

Keywords

  • Laparoscopic surgery
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In context

Lead sponsor

Western Galilee Hospital-Nahariya is the lead sponsor of 87 studies on the registry; 16 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Laparoscopic bariatric surgery
  • Laparoscopic inguinal hernia surgery

Exclusion criteria

Exclusion Criteria:

  • Cardiac arrythmias
  • Active ischemic heart disease
  • pregnancy
05

Study design

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

Study arms

  • Placebo comparator
    Ropivacaine

    Topical use of Ropivacaine

    Drug: Topical use · Other: laparoscopic repair of inguinal hernia · Other: laparoscopic bariatric surgery

  • Placebo comparator
    Placebo

    Topical use of placebo

    Drug: Topical use · Other: laparoscopic repair of inguinal hernia · Other: laparoscopic bariatric surgery

Interventions

  • DrugTopical use

    Topical use of Ropivacaine in laparoscopic surgery

    Also known as: Ropivacaine, Placebo

  • Otherlaparoscopic repair of inguinal hernia

    intra-operative treatment with ropivacaine Vs placebo in laparoscopic repair of inguinal hernia

  • Otherlaparoscopic bariatric surgery

    intra-operative treatment with ropivacaine Vs placebo in laparoscopic bariatric surgery

06

What researchers measure

Primary outcomes

  1. Pain scale as measured by pain scale questionnaire

    post operative pain intensity will be assisted by VAS(visual analog pain scale) scale at fixed times after surgery

    Time frame: 1 Week

Secondary outcomes

  1. Reducing use of narcotics according to nurse records

    patients will be treated by standard analgetic protocol, the records of analgetic drugs will be collected during patients hospitalization

    Time frame: 1 Week

07

Study locations

1 site
  • Naharia Medical Center
    Naharia, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 11, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02826876
Lead sponsor
Western Galilee Hospital-Nahariya
Responsible party
Farraj Moaad (Dr, Western Galilee Hospital-Nahariya) — Principal investigator
First posted
Jul 11, 2016
Start date
Jul 2016
Primary completion
Jul 2017 (estimated)
Completion
Jul 2017 (estimated)
Last update
Jul 11, 2016

Study contacts

Moaad H Farraj, Dr
Contact
moaad.farraj@naharia.health.gov.il
0507887996 ext. 972
Moaad H Farraj, Dr
principal investigator · Galilee 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 Jul 2016. You cannot join it, but the record below documents what was studied.

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