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Acromegaly Treatment Quality of Life Study

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Mass General Brigham

Status

Completed

Conditions

Acromegaly

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT01732406
2012P001556

Details and patient eligibility

About

The investigators hypothesize that treatment of acromegaly will be associated with an improvement in quality of life compared to active acromegaly. At the same time, they will also be studying the effects of different acromegaly treatments on the quality of life.

Enrollment

126 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-90
  • Active acromegaly or receiving pegvisomant monotherapy or receiving somatostatin analog monotherapy

Exclusion criteria

  • Untreated thyroid or adrenal insufficiency. Subjects on replacement therapy must be stable for at least 3 months prior to entry into the study
  • Initiation or discontinuation of testosterone or estrogen within 3 months of entry
  • Pregnant and nursing women

Trial design

126 participants in 3 patient groups

Acomegaly with Pegvisomant
Description:
Patients receiving pegvisomant monotherapy from own doctor to treat acromegaly.
Acromegaly with somatostatin analog
Description:
Patients receiving somatostatin analog monotherapy from own doctor to treat acromegaly
Active Acromegaly
Description:
Patients not on drugs for treatment of acromegaly

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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