The primary objective of this study is to evaluate the presence/absence and description of persistent sexual troubles following surgical treatment for endometriosis for women, and their partners.

Inclusion Criteria:

• The patient (and her partner) must have given his/her informed and signed consent
• The patient (and her partner) must be insured or beneficiary of a health insurance plan
• Couples for whom the woman has formerly undergone surgical treatment for endometriosis, and for the partner agrees to respond to questionnaires for this study

Exclusion Criteria:

• The patient (or her partner) is participating in another study
• The patient (or her partner) is in an exclusion period determined by a previous study
• The patient (or her partner) is under judicial protection, under tutorship or curatorship
• The patient (or her partner) refuses to sign the consent
• It is impossible to correctly inform the patient (or her partner)
• The patient is pregnant
• The patient is breastfeeding
• The patient was surgically treated for endometriosis, but was single.

Couples for whom the women have been surgically treated for deep endometriosis at the Nîmes University Hospital