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Sphenopalatine Ganglion Block to Treat Shoulder Pain During and/or After Cesarean

Sphenopalatine Ganglion Block to Treat Shoulder Pain During and/or After Cesarean

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02670057
Enrollment
117
Registered
2016-02-01
Start date
2015-11-30
Completion date
2017-12-12
Last updated
2017-12-14

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

Conditions

Ipsilateral Shoulder Pain

Brief summary

The purpose of this open label pilot study is to evaluate the utility of sphenopalatine ganglion (SPG) block to manage ipsilateral shoulder pain (ISP) during and/or after cesarean.

Detailed description

Shoulder pain thought to be caused by blood and amniotic fluid irritation of the diaphragm and nerves that supply the shoulder, can occur during and/or after a cesarean. Investigators will consent 100 patients, and will enroll 10 patients who develop ISP and have a score of is \>5/10 on the Verbal Analog pain Scale (VAS). Patients will be their own controls. Transnasal SPG block will be performed after childbirth, and and beginning at 20 minutes post treatment, the patient will be asked to rate their shoulder pain using the VAS a number of times.

Interventions

PROCEDURETransnasal SPG block

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Cesarean * Presence of post-operative ISP, VAS \>5/10 * American Society of Anesthesiologists Class 1 - 3. * No allergy to lidocaine

Exclusion criteria

* American Society of Anesthesiologists Class 4 or 5. * Allergy to lidocaine * Nasal pathology (e.g., deviated septum) * Patients who receive sedatives during cesarean * Bleeding diathesis * Any patient who the PI feels will be unable to comply with all protocol related procedures * Shoulder pain prior to cesarean

Design outcomes

Primary

MeasureTime frame
Reduction of shoulder pain measured using Verbal Analog pain Scale (VAS)90 Minutes

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026