A Study to Evaluate Cranioplasty Reconstruction Outcomes


About this study

The purpose of this study is to assess complications rates with different cranioplasty materials.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Patients who underwent cranioplasty reconstruction for various neurosurgical indications.
  • Follow up time of a minimum of 1 week after cranioplasty reconstruction.

Exclusion Criteria: 

  • Follow up time of less than 1 week after cranioplasty reconstruction.



Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Rochester, Minn.

Mayo Clinic principal investigator

Basel Sharaf, M.D., D.D.S.

Closed for enrollment

More information


Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

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