Local research. Human connections. WCR Miami Lakes (786) 483-7856
Back to study searchNCT07775053
CompletedNCT07775053ClinicalTrials.gov record

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

Postoperative Pain

THE QUICK READ

What this study involves

The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.

Study type
Interventional
Phase
Not applicable
Age range
20 years - 70 years
Sex eligible
All sexes
Healthy volunteers
Accepted
Participants
62 Actual

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

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

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

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:

1. Patients on anticoagulant therapy.
2. Patients with a BMI≥35 kg/m3.
3. Patients with a history of allergy to local anesthetics.
4. Patients with significant neurological or psychiatric disorders.
5. Pregnant patients.

Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Random assignment
Masking
Quadruple masked
Ropivacaine with tramadol

Not reported in this registry record.

Procedure: Pectoral Nerve Block

Ropivacaine Alone

Not reported in this registry record.

Procedure: Pectoral Nerve Block

Pectoral Nerve Block PROCEDURE

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

Pectoral Nerve Block PROCEDURE

This group will receive ropivacaine only.

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Postoperative Pain with visual analogue scale

Time frame: 24 hours postoperatively

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.

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Dr Faisal Masood teaching Hospital SargodhaSargodha, Punjab Province, PakistanStatus unknown

Study team and timeline

Lead sponsor
Sargodha Medical College
Study start
Jan 22, 2026 Actual
Primary completion
Mar 19, 2026 Actual
Study completion
Mar 19, 2026 Actual
First posted
Aug 20, 2026 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

No central contact is listed. Check the locations and the official record.

Official study title

Comparison of Post Operative Analgesia Between 0.25% Ropivacaine and 0.25% Ropivacaine Combined With Tramadol in Ultrasound Guided Modified Pectoral Nerve Block for Patient Undergoing Modified Radical Mastectomy.

A HUMAN NEXT STEP

Ask Wellness Clinical Research

Your message goes to WCR, including when this study is run by another organization. WCR may offer general guidance but may not operate this trial, have access to its team or be able to enroll you.

Please do not include medical records, diagnoses, medications, insurance numbers or other sensitive details. This form is for general questions, not urgent care.

Sending a question does not enroll you in a trial.

Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026