ClinicalTrials.gg
CompletedNCT07775053Updated Nov 10, 2026

Efficacy of Tramadol With Ropivacaine for Modified Pectoral Nerve Block in Breast Cancer Surgery

An interventional study of Pectoral Nerve Block and Pectoral Nerve Block in Postoperative Pain, sponsored by Sargodha Medical College. Completed at 1 site in Pakistan. Open to participants aged 20 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-10.

Sponsored by Sargodha Medical College · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Jan 2026, registered Aug 2026).
Updated Nov 10, 2026Now CompletedPrimary completion moved+2 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
62
Allocation
Randomized
Ages
20 Years to 70 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 134 studies in Pain, Postoperative with a site in Pakistan — 38 open to participants now, 41 under way, 5 of them phase 3. Pain, Postoperative · Pakistan.

Enrollment
90th of 132
62 · median 79
Started
2026
with 21 others
No phase
83 of 134
24 open now
Registered
120th of 134
by date
Lead sponsor
4 of 134
Sargodha Medical College

Among the 134 studies in Pain, Postoperative with a site in Pakistan, this one is the 90th largest by enrollment of the 132 interventional ones that give a count, is one of 22 that started in 2026, is one of 83 with no phase, and was the 120th registered.

Pain, Postoperative

5,640 studies on the registry are indexed under Pain, Postoperative; 1,230 are open to participants now.

Browse Pain, Postoperative studies →

Open to participants now

38 of the 134 studies in Pain, Postoperative with a site in Pakistan are open now. Recruiting first, the newest first:

33 more — sign in →

All 38 open studies →

A study can be open while its sites in Pakistan have not opened yet or have stopped. Only those recruiting at a site in Pakistan →

Who these studies take

Of the 679 Pain, Postoperative studies recruiting now, 241 (35%) set no upper age limit and 328 (48%) stop at 75 or younger; 74 take children under 18; 128 take healthy volunteers.

This study: 20 Years to 70 Years · all sexes · healthy volunteers too.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 134 studies in Pain, Postoperative with a site in Pakistan, or all of them as a file.
02

Study summary

In this study the investigators will compare the post operative opoid consumption for patient undergoing modified radical mastectomy. The patients will be divided into two groups one group will receive modified pectoral nerve block with local anesthetic ropivacaine combined with tramadol and other group will receive pectoral nerve block with ropivacaine only

03

Conditions studied

  • Postoperative Pain

Browse trials for

04

Who can participate

Ages eligible
20 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Female Patients aged 20-70 years
  2. Patients scheduled for elective unilateral modified radical mastectomy
  3. Patients with ASAI andII physical status.

Exclusion criteria

Exclusion Criteria:

  1. Patients on anticoagulant therapy.
  2. Patients with a ≥35 kg/m3.
  3. Patients with a history of allergy to local anesthetics.
  4. Patients with significant neurological or psychiatric disorders.
  5. Pregnant patients.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

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

Study arms

  • Other
    Ropivacaine with tramadol

    Procedure: Pectoral Nerve Block

  • Other
    Ropivacaine Alone

    Procedure: Pectoral Nerve Block

Interventions

  • ProcedurePectoral Nerve Block

    One group will receive ropivacaine with tramadol in modified pectoral nerve block

  • ProcedurePectoral Nerve Block

    This group will receive ropivacaine only.

06

What researchers measure

Primary outcomes

  1. Postoperative Pain with visual analogue scale

    Post operatively pain will be accessed by visual analogue scale . Visual analogue scale (VAS) scale has score from 0 to 10 where 0 score indicate no or minimal pain and score of 10 indicate worst possible pain.

    Time frame: 24 hours postoperatively

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jan 2026 to primary completion in Mar 2026, 1 month.

Of 2,089 non-industry interventional studies with no phase under Pain, Postoperative, half reached primary completion within 11 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 23. This study's 1 month is below that.

Counting every sponsor, half of 2,102 studies reached it within 11 months; a quarter within 6 and three quarters within 23.

Since we started tracking on Sep 25, 2026, the dates moved once, on Nov 10, 2026: primary completion Aug 2027 → Mar 2026 and completion Aug 2027 → Mar 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 15, 2026
First posted
Aug 20, 2026
StartActual
Jan 22, 2026
Primary completionActual
Mar 19, 2026was Aug 2027
CompletionActual
Mar 19, 2026was Aug 2027
Last update
Nov 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Status
Enrolling by invitation→Completed
changed Nov 10, 2026
Primary completion
Aug 2027→Mar 19, 2026 (actual)
Nov 10, 2026
Study completion
Aug 2027→Mar 19, 2026 (actual)
Nov 10, 2026
Show all 1 update
  1. Nov 10, 2026
    Enrolling by invitation→Completed
    Primary completion Aug 2027→Mar 19, 2026 (now actual)
    Study completion Aug 2027→Mar 19, 2026 (now actual)
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07775053
Lead sponsor
Sargodha Medical College
Responsible party
Sponsor
First posted
Aug 20, 2026
Start date
Jan 22, 2026
Primary completion
Mar 19, 2026
Completion
Mar 19, 2026
Last update
Nov 10, 2026

Oversight

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

Not currently enrolling

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

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Discussion

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