CompletedNot Applicable

Effect of Midazolam as Premedication in Patients Undergoing Breast Conservation Study

Pakistan124 participantsStarted 2024-08-30

Plain-language summary

Patient are randomized into 2 groups under computer registered numbers. Patient anxiety score is calculated through APAIS SCORE. Then one group is given Midazolam, and the other group is given normal saline and then after one day patients satisfaction is calculated through Lppsq scale.

Who can participate

Age range60 Years

SexFEMALE

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Inclusion criteria

✓. All patients undergoing breast conservation surgery
✓. ASA I-II

Exclusion criteria

✕. Patients already on anxiolytic medication
✕. Pregnancy
✕. Allergy to Midazolam,
✕. Patient with diagnosed psychosis,
✕. Chronic kidney disease.

What they're measuring

Comparison of frequency of patient satisfaction & anxiety

Timeframe: 1 day

Trial details

NCT IDNCT07184125

SponsorShaukat Khanum Memorial Cancer Hospital & Research Centre

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-09-10

View on ClinicalTrials.gov More Anxiety trials