Efficacy of Tramadol With Ropivacaine for Modified Pectoral Nerve Block in Breast Cancer Surgery
Postoperative Pain
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.
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.
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.
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.
Ask Wellness Clinical Research
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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
