Efficacy of Ultrasound guided PECS block with Magnesium sulfate

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201707002376424

Enrollment

Registered

2017-06-26

Start date

2015-05-26

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Cancer Surgery POSTOPERATIVE MASTECTOMY PAIN

Interventions

Group C

Group B

Group M

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 90 adult female with patients physical status ASA classes I , II and III,

Exclusion criteria

Exclusion criteria: Exclusion criteria included refusal of the patients, contraindications to regional anesthesia (including coagulopathy and local infection, fungating breast cancer), history of allergy to the medications used in the study, patient with history of drug abuse, prior breast surgery except for diagnostic biopsies, and history of treatment for a chronic pain condition, and/or psychiatric disorder.

Design outcomes

Primary

Measure	Time frame
This study aimed to compare the intraoperative hemodynamic changes, postoperative analgesia, postoperative sedation, and postoperative side effects of the PECS procedure with and without Magnesium sulfate	—

Secondary

Measure	Time frame
to improve the postoperative outcome and this will reduce the postoperative complication	—

Countries

Egypt

Contacts

Public ContactHatem Abo el wafa

lecturer of anesthesia, Menoufia university

hatem_wafa@hotmail.com00201155497711

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026