Rectal diclofenac in day care breast surgery

Efficacy of preemptive analgesia using rectal diclofenac among patients undergoing breast surgery in day care : A randomized control study - Reclo Study

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/09/015695

Enrollment

Registered

2018-09-12

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N60-N65- Disorders of breast

Interventions

Intervention1: Rectal diclofenac suppository Vs Placebo: Comparision of rectal diclofenac suppository vs Placebo in Post op analgesi in Breast surgery patients in day care Control Intervention1: Place

Eligibility

Inclusion criteria

Inclusion criteria: All patients undergoing breast surgery in Day care under general anesthesia

Exclusion criteria

Exclusion criteria: Patients with history of Peptic ulcer disease, chronic kidney disease, bronchial asthma and liver disease

Design outcomes

Primary

Measure	Time frame
To assess efficacy of preemptive analgesia using rectal diclofenac among patients undergoing breast surgery in day care facilityTimepoint: Immediate post operative period	—

Secondary

Measure	Time frame
Secondarily the time interval between extubation and need for rescue analgesia if required is also calculated. If the participant does not ask for rescue analgesia, analgesic is given only at discharge and the same will be noted in the proformaTimepoint: Immediate post operative period	—

Countries

India

Contacts

Public ContactArelly Samuel Paul Dhinakar

Christian Medical College, Vellore

vabraham@cmcvellore.ac.in8009929986

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026